AmBeed is committed to providing customers with high-quality inhibitors/agonists, antibodies, fluorescent dyes, antibiotics and other diversified products, covering more than 70,000 life science research-related products, to meet the needs of customers in biochemistry, molecular biology, protein science, cell biology, microbiology and drug discovery and other fields. In the face of the ever-evolving scientific field, we always actively listen to the voice of our customers, constantly absorb feedback and optimize the product line to ensure that our products always keep up with the needs of industry development and create more value for customers.
AmBeed INC provides upto 6719 kinds of products, to contact us please scan the QRcode or click on the button below
Product Category
Inhibitors|Agonists 6677Natural product 17Cancer 11Biochemical reagent 7PROTAC 3Cell Biology 2Pharmaceutical Research 1Animal Modeling Reagent 1
Featured Products
CAS: 88899-55-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg
Package: A614767
Price: 1089, 7250, 1764 (in RMB)
Descriptions: Bafilomycin A1 is an inhibitor of vacuolar H+-ATPase with IC50 of 0.44 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg
Package: A614767
Price: 1089, 7250, 1764 (in RMB)
Descriptions: Bafilomycin A1 is an inhibitor of vacuolar H+-ATPase with IC50 of 0.44 nM.
Last Update: 2026-04-17 13:46:08
CAS: 256373-96-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A110681
Price: 109, 462, 315, 378, 553, 1197, 2016, 2505, 5796, 8101 (in RMB)
Descriptions: MCC950 sodium (CRID3 sodium salt) is an effective and selective NLRP3 inhibitor with IC50 values of 7.5 nM in BMDMs and 8.1 nM in HMDMs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A110681
Price: 109, 462, 315, 378, 553, 1197, 2016, 2505, 5796, 8101 (in RMB)
Descriptions: MCC950 sodium (CRID3 sodium salt) is an effective and selective NLRP3 inhibitor with IC50 values of 7.5 nM in BMDMs and 8.1 nM in HMDMs.
Last Update: 2026-04-17 13:46:08
CAS: 866405-64-3
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A137399
Price: 119, 500, 163, 456, 665, 1358, 2170, 2930 (in RMB)
Descriptions: Dorsomorphin is a selective, ATP-competitive AMPK inhibitor (Ki of 109 nM in the absence of AMP) that selectively inhibits BMP type I receptors ALK2, ALK3, and ALK6, and reverses autophagy activation and anti-inflammatory effects induced by Urolithin A.Dorsomorphin promotes differentiation of human pluripotent stem cells into neural progenitor cells, promotes differentiation of both mouse and human pluripotent stem cells into cardiomyocytes, enhances adipogenic differentiation of human mesenchymal cells, and inhibits osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A137399
Price: 119, 500, 163, 456, 665, 1358, 2170, 2930 (in RMB)
Descriptions: Dorsomorphin is a selective, ATP-competitive AMPK inhibitor (Ki of 109 nM in the absence of AMP) that selectively inhibits BMP type I receptors ALK2, ALK3, and ALK6, and reverses autophagy activation and anti-inflammatory effects induced by Urolithin A.Dorsomorphin promotes differentiation of human pluripotent stem cells into neural progenitor cells, promotes differentiation of both mouse and human pluripotent stem cells into cardiomyocytes, enhances adipogenic differentiation of human mesenchymal cells, and inhibits osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 15663-27-1
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A210558
Price: 100, 116, 164, 232, 348, 918, 1543 (in RMB)
Descriptions: Cisplatin (CDDP) is an antitumor chemotherapeutic agent that induces DNA damage in cancer cells through DNA cross-linking. Cisplatin can activate ferroptosis and induce autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A210558
Price: 100, 116, 164, 232, 348, 918, 1543 (in RMB)
Descriptions: Cisplatin (CDDP) is an antitumor chemotherapeutic agent that induces DNA damage in cancer cells through DNA cross-linking. Cisplatin can activate ferroptosis and induce autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 1219168-18-9
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A213616
Price: 139, 716, 203, 410, 598, 1380, 1960 (in RMB)
Descriptions: Dorsomorphin 2HCl is an AMPK inhibitor with an Ki value of 109 nM for AMPK. Dorsomorphin 2HCl inhibits the BMP signaling pathway and can be used in research on stem cell differentiation and bone regeneration.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A213616
Price: 139, 716, 203, 410, 598, 1380, 1960 (in RMB)
Descriptions: Dorsomorphin 2HCl is an AMPK inhibitor with an Ki value of 109 nM for AMPK. Dorsomorphin 2HCl inhibits the BMP signaling pathway and can be used in research on stem cell differentiation and bone regeneration.
Last Update: 2026-04-17 13:46:08
CAS: 58-58-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A547954
Price: 259, 384, 751, 1417, 2667 (in RMB)
Descriptions: Puromycin 2HCl is an aminonucleoside antibiotic that acts as a protein synthesis inhibitor in mammalian cell lines selectively expressing transfected with the pac gene (Streptomyces alboa), and its product, puromycin acetyltransferase, inactivates the drug by acetylation, inducing intracellular DNA fragmentation in thymocytes and HL-60 leukemia. (The recommended range for transfection of mammalian cells is 1-30 μg/ml.)
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A547954
Price: 259, 384, 751, 1417, 2667 (in RMB)
Descriptions: Puromycin 2HCl is an aminonucleoside antibiotic that acts as a protein synthesis inhibitor in mammalian cell lines selectively expressing transfected with the pac gene (Streptomyces alboa), and its product, puromycin acetyltransferase, inactivates the drug by acetylation, inducing intracellular DNA fragmentation in thymocytes and HL-60 leukemia. (The recommended range for transfection of mammalian cells is 1-30 μg/ml.)
Last Update: 2026-04-17 13:46:08
CAS: 347174-05-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A228648
Price: 119, 508, 179, 416, 725, 1544, 2646, 3969 (in RMB)
Descriptions: Ferrostatin-1 is a ferroptosis inhibitor with an IC50 value of 60 nM. Ferrostatin-1 has neuroprotective and antitumor effects and can be used in research on the role of ferroptosis in neurodegenerative diseases and cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A228648
Price: 119, 508, 179, 416, 725, 1544, 2646, 3969 (in RMB)
Descriptions: Ferrostatin-1 is a ferroptosis inhibitor with an IC50 value of 60 nM. Ferrostatin-1 has neuroprotective and antitumor effects and can be used in research on the role of ferroptosis in neurodegenerative diseases and cancer.
Last Update: 2026-04-17 13:46:08
CAS: 210826-40-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A448777
Price: 150, 420, 665, 1365, 2240, 2783, 7791 (in RMB)
Descriptions: MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM in BMDMs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A448777
Price: 150, 420, 665, 1365, 2240, 2783, 7791 (in RMB)
Descriptions: MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM in BMDMs.
Last Update: 2026-04-17 13:46:08
CAS: 167869-21-8
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A282482
Price: 129, 685, 233, 472, 682, 1953, 2583 (in RMB)
Descriptions: PD98059 is a non-ATP-competitive MEK inhibitor with IC50 values of 2-7 μM for MEK1 and 50 μM for MEK2, inhibiting MAPK activation and TCDD binding.PD98059 prevents differentiation of mouse ES cells, enhances adipogenic differentiation of human mesenchymal stem cells, and inhibits their osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A282482
Price: 129, 685, 233, 472, 682, 1953, 2583 (in RMB)
Descriptions: PD98059 is a non-ATP-competitive MEK inhibitor with IC50 values of 2-7 μM for MEK1 and 50 μM for MEK2, inhibiting MAPK activation and TCDD binding.PD98059 prevents differentiation of mouse ES cells, enhances adipogenic differentiation of human mesenchymal stem cells, and inhibits their osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 53123-88-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A656002
Price: 109, 424, 216, 346, 472, 693, 945, 1572, 2394, 3724 (in RMB)
Descriptions: Rapamycin is a specific mTOR inhibitor with IC50 of ~0.1 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A656002
Price: 109, 424, 216, 346, 472, 693, 945, 1572, 2394, 3724 (in RMB)
Descriptions: Rapamycin is a specific mTOR inhibitor with IC50 of ~0.1 nM.
Last Update: 2026-04-17 13:46:08
CAS: 846557-71-9
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A722849
Price: 119, 591, 189, 472, 819, 1512, 2419, 3874 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A722849
Price: 119, 591, 189, 472, 819, 1512, 2419, 3874 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
CAS: 243984-11-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A888245
Price: 149, 847, 346, 693, 1071, 2590, 3654, 6237 (in RMB)
Descriptions: TAK-242, a small-molecule-specific inhibitor of Toll-like receptor (TLR)4 signaling, inhibits the production of lipopolysaccharide-induced inflammatory mediators by binding to the intracellular domain of TLR4.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A888245
Price: 149, 847, 346, 693, 1071, 2590, 3654, 6237 (in RMB)
Descriptions: TAK-242, a small-molecule-specific inhibitor of Toll-like receptor (TLR)4 signaling, inhibits the production of lipopolysaccharide-induced inflammatory mediators by binding to the intracellular domain of TLR4.
Last Update: 2026-04-17 13:46:08
CAS: 50-02-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A144976
Price: 109, 208, 110, 165, 245, 350, 586, 1432 (in RMB)
Descriptions: Dexamethasone results in decrease in transmonolayer paracellular permeability mainly to sucrose, fluorescein and dextrans of up to 20 KDa in an immortalised rat brain endothelial cell line (GPNT).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A144976
Price: 109, 208, 110, 165, 245, 350, 586, 1432 (in RMB)
Descriptions: Dexamethasone results in decrease in transmonolayer paracellular permeability mainly to sucrose, fluorescein and dextrans of up to 20 KDa in an immortalised rat brain endothelial cell line (GPNT).
Last Update: 2026-04-17 13:46:08
CAS: 1032350-13-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A145592
Price: 129, 629, 261, 595, 820, 1418, 2030, 2870, 5166 (in RMB)
Descriptions: MK-2206 2HCl is a selective AKT inhibitor with IC50 values of 8 nM, 12 nM, and 65 nM for AKT1, AKT2, and AKT3, respectively. MK-2206 2HCl exhibits antitumor effects and is used in research on cancers related to the PI3K/AKT signaling pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A145592
Price: 129, 629, 261, 595, 820, 1418, 2030, 2870, 5166 (in RMB)
Descriptions: MK-2206 2HCl is a selective AKT inhibitor with IC50 values of 8 nM, 12 nM, and 65 nM for AKT1, AKT2, and AKT3, respectively. MK-2206 2HCl exhibits antitumor effects and is used in research on cancers related to the PI3K/AKT signaling pathway.
Last Update: 2026-04-17 13:46:08
CAS: 19542-67-7
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A107077
Price: 109, 385, 315, 409, 1386, 1890 (in RMB)
Descriptions: BAY 11-7082 is an inhibitor of IκBα phosphorylation and NF-κB. It selectively and irreversibly inhibits TNF-α-induced phosphorylation of IκB-α, decreases NF-κB activity, and reduces the expression of adhesion molecules. Additionally, BAY 11-7082 inhibits ubiquitin-specific proteases USP7 and USP21 (IC50 = 0.19, 0.96 μM, respectively), gasdermin D (GSDMD) pore formation in liposomes, and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A107077
Price: 109, 385, 315, 409, 1386, 1890 (in RMB)
Descriptions: BAY 11-7082 is an inhibitor of IκBα phosphorylation and NF-κB. It selectively and irreversibly inhibits TNF-α-induced phosphorylation of IκB-α, decreases NF-κB activity, and reduces the expression of adhesion molecules. Additionally, BAY 11-7082 inhibits ubiquitin-specific proteases USP7 and USP21 (IC50 = 0.19, 0.96 μM, respectively), gasdermin D (GSDMD) pore formation in liposomes, and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells.
Last Update: 2026-04-17 13:46:08
CAS: 146986-50-7
Category: Inhibitors|Agonists, Cell Culture
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A112358
Price: 252, 599, 760, 1865, 2665, 4799 (in RMB)
Descriptions: Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II with Ki values of 220 nM and 300 nM, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A112358
Price: 252, 599, 760, 1865, 2665, 4799 (in RMB)
Descriptions: Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II with Ki values of 220 nM and 300 nM, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 51-21-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A370752
Price: 109, 350, 158, 228, 283, 529 (in RMB)
Descriptions: 5-Fluorouracil is a potent antitumor compound that inhibits thymidylate synthase, depleting the intracellular dTTP pool by interfering with pyrimidine synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A370752
Price: 109, 350, 158, 228, 283, 529 (in RMB)
Descriptions: 5-Fluorouracil is a potent antitumor compound that inhibits thymidylate synthase, depleting the intracellular dTTP pool by interfering with pyrimidine synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 154-17-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A104420
Price: 153, 210, 252, 315, 938, 1490 (in RMB)
Descriptions: 2-Deoxy-D-glucose is a glucose analog that inhibits glycolysis by targeting hexokinase.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A104420
Price: 153, 210, 252, 315, 938, 1490 (in RMB)
Descriptions: 2-Deoxy-D-glucose is a glucose analog that inhibits glycolysis by targeting hexokinase.
Last Update: 2026-04-17 13:46:08
CAS: 5142-23-4
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50mg, 100mg, 250mg, 500mg
Package: A145872
Price: 346, 504, 910, 1764 (in RMB)
Descriptions: 3-Methyladenine is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC50 of 25 μM and 60 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50mg, 100mg, 250mg, 500mg
Package: A145872
Price: 346, 504, 910, 1764 (in RMB)
Descriptions: 3-Methyladenine is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC50 of 25 μM and 60 μM.
Last Update: 2026-04-17 13:46:08
CAS: 305834-79-1
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A261312
Price: 109, 303, 170, 378, 598, 1750, 2450, 3711 (in RMB)
Descriptions: SC79 is a specific Akt agonist capable of crossing the blood-brain barrier. It activates cytosolic Akt and inhibits Akt membrane translocation by specifically binding to the PH domain of Akt.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A261312
Price: 109, 303, 170, 378, 598, 1750, 2450, 3711 (in RMB)
Descriptions: SC79 is a specific Akt agonist capable of crossing the blood-brain barrier. It activates cytosolic Akt and inhibits Akt membrane translocation by specifically binding to the PH domain of Akt.
Last Update: 2026-04-17 13:46:08
CAS: 1173097-76-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A132258
Price: 119, 595, 295, 473, 769, 1323, 2171, 3128 (in RMB)
Descriptions: U0126 (U0126-EtOH) is a potent, non-ATP competitive, and selective MEK1 and MEK2 inhibitor with IC50 values of 72 nM and 58 nM, respectively. It also inhibits autophagy and mitophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A132258
Price: 119, 595, 295, 473, 769, 1323, 2171, 3128 (in RMB)
Descriptions: U0126 (U0126-EtOH) is a potent, non-ATP competitive, and selective MEK1 and MEK2 inhibitor with IC50 values of 72 nM and 58 nM, respectively. It also inhibits autophagy and mitophagy.
Last Update: 2026-04-17 13:46:08
CAS: 154447-36-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A133122
Price: 119, 501, 409, 598, 1086, 1418, 1953, 5103 (in RMB)
Descriptions: LY294002 is a PI3K inhibitor with IC50 values of 0.5 μM for PI3Kα, 0.57 μM for PI3Kδ, and 0.97 μM for PI3Kβ. LY294002 has anti-tumor effects and is used to study the PI3K/AKT signaling pathway and related cancer treatments. LY294002 promotes the differentiation of mouse embryonic stem cells into insulin-producing cells and inhibits the fusion of myoblasts into myotubes.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A133122
Price: 119, 501, 409, 598, 1086, 1418, 1953, 5103 (in RMB)
Descriptions: LY294002 is a PI3K inhibitor with IC50 values of 0.5 μM for PI3Kα, 0.57 μM for PI3Kδ, and 0.97 μM for PI3Kβ. LY294002 has anti-tumor effects and is used to study the PI3K/AKT signaling pathway and related cancer treatments. LY294002 promotes the differentiation of mouse embryonic stem cells into insulin-producing cells and inhibits the fusion of myoblasts into myotubes.
Last Update: 2026-04-17 13:46:08
CAS: 54-05-7
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A136097
Price: 109, 385, 220, 315, 560, 1103 (in RMB)
Descriptions: Chloroquine is an antimalarial drug and also an autophagy inhibitor, with an IC50 value of 2.1 μM for inhibiting autophagy. Chloroquine has antimalarial, anti-inflammatory, and antitumor effects and can be used in research on autophagy and malaria treatment.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A136097
Price: 109, 385, 220, 315, 560, 1103 (in RMB)
Descriptions: Chloroquine is an antimalarial drug and also an autophagy inhibitor, with an IC50 value of 2.1 μM for inhibiting autophagy. Chloroquine has antimalarial, anti-inflammatory, and antitumor effects and can be used in research on autophagy and malaria treatment.
Last Update: 2026-04-17 13:46:08
CAS: 152121-47-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A248150
Price: 109, 288, 263, 420, 685, 980, 1470, 1980 (in RMB)
Descriptions: SB 203580 is a selective p38 MAPK inhibitor with IC50 values of 50 nM for SAPK2a/p38 and 500 nM for SAPK2b/p38β2, without inhibiting JNK activity. It can activate autophagy and mitophagy. SB203580 enhances cardiomyocyte differentiation from human embryonic stem cells but inhibits cardiomyocyte differentiation from mouse embryonic stem cells by suppressing early mesoderm formation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A248150
Price: 109, 288, 263, 420, 685, 980, 1470, 1980 (in RMB)
Descriptions: SB 203580 is a selective p38 MAPK inhibitor with IC50 values of 50 nM for SAPK2a/p38 and 500 nM for SAPK2b/p38β2, without inhibiting JNK activity. It can activate autophagy and mitophagy. SB203580 enhances cardiomyocyte differentiation from human embryonic stem cells but inhibits cardiomyocyte differentiation from mouse embryonic stem cells by suppressing early mesoderm formation.
Last Update: 2026-04-17 13:46:08
CAS: 338967-87-6
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A252480
Price: 109, 350, 252, 405, 791, 1379, 1930 (in RMB)
Descriptions: Mdivi-1 selectively inhibits mitochondrial division DRP1 and mitochondrial division Dynamin I (Dnm1), the IC50 is about 1-10 µM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A252480
Price: 109, 350, 252, 405, 791, 1379, 1930 (in RMB)
Descriptions: Mdivi-1 selectively inhibits mitochondrial division DRP1 and mitochondrial division Dynamin I (Dnm1), the IC50 is about 1-10 µM.
Last Update: 2026-04-17 13:46:08
CAS: 1797989-42-4
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A219562
Price: 129, 616, 378, 504, 693, 1470, 1764, 3465 (in RMB)
Descriptions: Laduviglusib monohydrochloride is a selective GSK-3 inhibitor with high affinity for GSK-3α and GSK-3β, with IC50 values of 2.2 nM and 1.5 nM, respectively. Laduviglusib has neuroprotective and anticancer effects and can be used in research on Alzheimer's disease and cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A219562
Price: 129, 616, 378, 504, 693, 1470, 1764, 3465 (in RMB)
Descriptions: Laduviglusib monohydrochloride is a selective GSK-3 inhibitor with high affinity for GSK-3α and GSK-3β, with IC50 values of 2.2 nM and 1.5 nM, respectively. Laduviglusib has neuroprotective and anticancer effects and can be used in research on Alzheimer's disease and cancer.
Last Update: 2026-04-17 13:46:08
CAS: 49843-98-3
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A142021
Price: 109, 370, 302, 403, 693, 1197, 1730 (in RMB)
Descriptions: EX-527 is a potent and selective SIRT1 inhibitor with IC50 of 38 nM, exhibits > 200-fold selectivity against SIRT2 and SIRT3.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A142021
Price: 109, 370, 302, 403, 693, 1197, 1730 (in RMB)
Descriptions: EX-527 is a potent and selective SIRT1 inhibitor with IC50 of 38 nM, exhibits > 200-fold selectivity against SIRT2 and SIRT3.
Last Update: 2026-04-17 13:46:08
CAS: 763113-22-0
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A134565
Price: 109, 397, 225, 361, 616, 910, 1386, 2495, 3465, 5198 (in RMB)
Descriptions: Olaparib is a PARP inhibitor with high affinity for PARP1 and PARP2, with IC50 values of 5 nM and 1 nM, respectively. Olaparib has antitumor effects and can be used in research on BRCA mutation-associated cancers.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A134565
Price: 109, 397, 225, 361, 616, 910, 1386, 2495, 3465, 5198 (in RMB)
Descriptions: Olaparib is a PARP inhibitor with high affinity for PARP1 and PARP2, with IC50 values of 5 nM and 1 nM, respectively. Olaparib has antitumor effects and can be used in research on BRCA mutation-associated cancers.
Last Update: 2026-04-17 13:46:08
CAS: 33069-62-4
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A238238
Price: 109, 400, 205, 328, 567, 945, 2450, 3800 (in RMB)
Descriptions: Paclitaxel is a natural antitumor drug that stabilizes the polymerization of tubulin, causing mitotic arrest and inducing apoptosis, ultimately leading to cell death. Paclitaxel also induces autophagy. Paclitaxel inhibits the initiation and growth of neurites in vitro by promoting microtubule polymerization.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A238238
Price: 109, 400, 205, 328, 567, 945, 2450, 3800 (in RMB)
Descriptions: Paclitaxel is a natural antitumor drug that stabilizes the polymerization of tubulin, causing mitotic arrest and inducing apoptosis, ultimately leading to cell death. Paclitaxel also induces autophagy. Paclitaxel inhibits the initiation and growth of neurites in vitro by promoting microtubule polymerization.
Last Update: 2026-04-17 13:46:08
CAS: 869185-85-3
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 50mg, 100mg
Package: A593990
Price: 231, 420, 980, 1470 (in RMB)
Descriptions: SB-203580 HCl is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 50mg, 100mg
Package: A593990
Price: 231, 420, 980, 1470 (in RMB)
Descriptions: SB-203580 HCl is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM.
Last Update: 2026-04-17 13:46:08
CAS: 129-56-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 250mg, 500mg
Package: A155219
Price: 109, 424, 216, 347, 535, 787, 1465, 2929 (in RMB)
Descriptions: SP600125 is a selective JNK inhibitor with high affinity for JNK1, JNK2, and JNK3, with IC50 values of 40 nM, 50 nM, and 90 nM, respectively. SP600125 has anti-inflammatory and antitumor effects and can be used in research on diseases related to the JNK signaling pathway.SP600125 inhibits BMP9-induced osteogenic differentiation of cultured mouse mesenchymal stem cells (MSCs) and primary bone marrow stromal cells, promotes adipogenic differentiation of human MSCs, but inhibits their osteogenic differentiation. When added during early stages of neuronal culture, SP600125 causes cell death and suppresses neurogenesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 250mg, 500mg
Package: A155219
Price: 109, 424, 216, 347, 535, 787, 1465, 2929 (in RMB)
Descriptions: SP600125 is a selective JNK inhibitor with high affinity for JNK1, JNK2, and JNK3, with IC50 values of 40 nM, 50 nM, and 90 nM, respectively. SP600125 has anti-inflammatory and antitumor effects and can be used in research on diseases related to the JNK signaling pathway.SP600125 inhibits BMP9-induced osteogenic differentiation of cultured mouse mesenchymal stem cells (MSCs) and primary bone marrow stromal cells, promotes adipogenic differentiation of human MSCs, but inhibits their osteogenic differentiation. When added during early stages of neuronal culture, SP600125 causes cell death and suppresses neurogenesis.
Last Update: 2026-04-17 13:46:08
CAS: 129830-38-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A101744
Price: 119, 539, 300, 700, 900, 1740, 3200, 5800, 7600, 10800 (in RMB)
Descriptions: Y-27632 dihydrochloride is an ATP-competitive ROCK inhibitor with oral bioactivity. Y-27632 dihydrochloride has anti-epileptic properties .
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A101744
Price: 119, 539, 300, 700, 900, 1740, 3200, 5800, 7600, 10800 (in RMB)
Descriptions: Y-27632 dihydrochloride is an ATP-competitive ROCK inhibitor with oral bioactivity. Y-27632 dihydrochloride has anti-epileptic properties .
Last Update: 2026-04-17 13:46:08
CAS: 4311-88-0
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A181851
Price: 119, 550, 281, 450, 945, 1254 (in RMB)
Descriptions: Necrostatin-1 is an inhibitor of RIP1 and can decrease TNF-α-induced necroptosis with EC50 of 490 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A181851
Price: 119, 550, 281, 450, 945, 1254 (in RMB)
Descriptions: Necrostatin-1 is an inhibitor of RIP1 and can decrease TNF-α-induced necroptosis with EC50 of 490 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1219810-16-8
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg, 1g
Package: A108537
Price: 169, 1019, 399, 665, 1050, 1575, 2520, 3276, 4914, 7585 (in RMB)
Descriptions: RSL3 ((1S,3R)-RSL3) is an inhibitor of glutathione peroxidase 4 (GPX4), which reduces GPX4 expression and induces ferroptosis in head and neck cancer cells. In HN3 resistant cells, it increases the protein levels of p62 and Nrf2, leading to Keap1 inactivation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg, 1g
Package: A108537
Price: 169, 1019, 399, 665, 1050, 1575, 2520, 3276, 4914, 7585 (in RMB)
Descriptions: RSL3 ((1S,3R)-RSL3) is an inhibitor of glutathione peroxidase 4 (GPX4), which reduces GPX4 expression and induces ferroptosis in head and neck cancer cells. In HN3 resistant cells, it increases the protein levels of p62 and Nrf2, leading to Keap1 inactivation.
Last Update: 2026-04-17 13:46:08
CAS: 252917-06-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A133052
Price: 139, 788, 243, 409, 693, 1134, 1921, 2822, 4082 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) is an effective, selective, and orally active GSK-3α/β inhibitor used as an auxiliary agent in cell therapy.CHIR99021 promotes the differentiation of human induced pluripotent stem cells (iPSCs) into insulin-producing cells and the differentiation of human ES and iPS cells into cardiomyocytes.When used in combination with SB431542 and human recombinant LIF, CHIR99021 supports the generation and maintenance of primitive neural stem cells from human ES cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A133052
Price: 139, 788, 243, 409, 693, 1134, 1921, 2822, 4082 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) is an effective, selective, and orally active GSK-3α/β inhibitor used as an auxiliary agent in cell therapy.CHIR99021 promotes the differentiation of human induced pluripotent stem cells (iPSCs) into insulin-producing cells and the differentiation of human ES and iPS cells into cardiomyocytes.When used in combination with SB431542 and human recombinant LIF, CHIR99021 supports the generation and maintenance of primitive neural stem cells from human ES cells.
Last Update: 2026-04-17 13:46:08
CAS: 571203-78-6
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A145112
Price: 315, 408, 960, 1488, 3630 (in RMB)
Descriptions: Erastin is a compound that interacts with VDAC, blocks and reverses mitochondrial depolarization after microtubule destabilizers in intact cells and antagonized tubulin-induced VDAC blockage in planar bilayers. It is also a ferroptosis inducer. (Unstable in solution, please prepare and use now).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A145112
Price: 315, 408, 960, 1488, 3630 (in RMB)
Descriptions: Erastin is a compound that interacts with VDAC, blocks and reverses mitochondrial depolarization after microtubule destabilizers in intact cells and antagonized tubulin-induced VDAC blockage in planar bilayers. It is also a ferroptosis inducer. (Unstable in solution, please prepare and use now).
Last Update: 2026-04-17 13:46:08
CAS: 109511-58-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A807258
Price: 169, 1056, 840, 1344, 2419, 3626 (in RMB)
Descriptions: U0126 is a highly selective inhibitor of both MEK1 and MEK2, a type of MAPK/ERK kinase. U-0126, when used in combination with FGF, Activin A, and PKC inhibitors, supports maintenance of human pluripotent stem cells, inhibits self-renewal, and leads to differentiation without affecting proliferation or survival.U-0126 also inhibits glutamate-induced oxidative stress in mouse hippocampal HT22 cells and primary rat cortical cultures and shows neuroprotective effects in a gerbil ischemia model and in hypoxic cultures of mouse primary neurons.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A807258
Price: 169, 1056, 840, 1344, 2419, 3626 (in RMB)
Descriptions: U0126 is a highly selective inhibitor of both MEK1 and MEK2, a type of MAPK/ERK kinase. U-0126, when used in combination with FGF, Activin A, and PKC inhibitors, supports maintenance of human pluripotent stem cells, inhibits self-renewal, and leads to differentiation without affecting proliferation or survival.U-0126 also inhibits glutamate-induced oxidative stress in mouse hippocampal HT22 cells and primary rat cortical cultures and shows neuroprotective effects in a gerbil ischemia model and in hypoxic cultures of mouse primary neurons.
Last Update: 2026-04-17 13:46:08
CAS: 25316-40-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg, 1g
Package: A130952
Price: 139, 792, 745, 1320, 2520, 3180, 4210 (in RMB)
Descriptions: Doxorubicin HCl is an effective inhibitor of DNA topoisomerase I and II, with IC50 values of 0.8 μM and 2.67 μM, respectively. Doxorubicin HCl has cytotoxic properties and induces apoptosis and autophagy, making it a widely used chemotherapeutic agent in cancer treatment.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg, 1g
Package: A130952
Price: 139, 792, 745, 1320, 2520, 3180, 4210 (in RMB)
Descriptions: Doxorubicin HCl is an effective inhibitor of DNA topoisomerase I and II, with IC50 values of 0.8 μM and 2.67 μM, respectively. Doxorubicin HCl has cytotoxic properties and induces apoptosis and autophagy, making it a widely used chemotherapeutic agent in cancer treatment.
Last Update: 2026-04-17 13:46:08
CAS: 161401-82-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A834991
Price: 359, 2375, 700, 2468, 4216 (in RMB)
Descriptions: Z-VAD-FMK (Z-VAD(OH)-FMK) is a pan caspase inhibitor. Z-VAD-FMK does not inhibit the activity of ubiquitin C-terminal hydrolase L1 (UCHL1) even at concentrations up to 440 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A834991
Price: 359, 2375, 700, 2468, 4216 (in RMB)
Descriptions: Z-VAD-FMK (Z-VAD(OH)-FMK) is a pan caspase inhibitor. Z-VAD-FMK does not inhibit the activity of ubiquitin C-terminal hydrolase L1 (UCHL1) even at concentrations up to 440 μM.
Last Update: 2026-04-17 13:46:08
CAS: 301836-41-9
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172016
Price: 129, 616, 350, 560, 2366, 3549 (in RMB)
Descriptions: SB-431542 is a TGF-β receptor kinase inhibitor (TRKI) in SMAD signaling.SB431542, in combination with LDN193189 or Noggin, promotes the differentiation of human pluripotent stem cell-derived neural progenitor cells, enhances proliferation and sheet formation of endothelial cells derived from mouse ES cells, boosts the differentiation of mouse and human pluripotent stem cells into cardiomyocytes, inhibits self-renewal of human pluripotent stem cells (PSCs), and induces their differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172016
Price: 129, 616, 350, 560, 2366, 3549 (in RMB)
Descriptions: SB-431542 is a TGF-β receptor kinase inhibitor (TRKI) in SMAD signaling.SB431542, in combination with LDN193189 or Noggin, promotes the differentiation of human pluripotent stem cell-derived neural progenitor cells, enhances proliferation and sheet formation of endothelial cells derived from mouse ES cells, boosts the differentiation of mouse and human pluripotent stem cells into cardiomyocytes, inhibits self-renewal of human pluripotent stem cells (PSCs), and induces their differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 16561-29-8
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A175370
Price: 239, 1519, 436, 1050, 1770, 3730 (in RMB)
Descriptions: Phorbol 12-myristate 13-acetate is a PKC-activating phorbol ester, increases the intracellular Ca2+ concentration ([Ca2+]i) in a dose-dependent manner, with an EC50 of 11.7 nM.Phorbol 12-myristate 13-acetate stimulates cardiac differentiation of mesenchymal stem cells and promotes hematopoietic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A175370
Price: 239, 1519, 436, 1050, 1770, 3730 (in RMB)
Descriptions: Phorbol 12-myristate 13-acetate is a PKC-activating phorbol ester, increases the intracellular Ca2+ concentration ([Ca2+]i) in a dose-dependent manner, with an EC50 of 11.7 nM.Phorbol 12-myristate 13-acetate stimulates cardiac differentiation of mesenchymal stem cells and promotes hematopoietic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 1268524-70-4
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A529842
Price: 129, 655, 588, 770, 1360, 1575, 2520, 3600 (in RMB)
Descriptions: (+)-JQ-1 (JQ1) is a potent, specific, and reversible BET bromodomain inhibitor, with IC50s of 77 and 33 nM for the first and second bromodomains (BRD4(1/2)). It also activates autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A529842
Price: 129, 655, 588, 770, 1360, 1575, 2520, 3600 (in RMB)
Descriptions: (+)-JQ-1 (JQ1) is a potent, specific, and reversible BET bromodomain inhibitor, with IC50s of 77 and 33 nM for the first and second bromodomains (BRD4(1/2)). It also activates autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 50-63-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg
Package: A233637
Price: 99, 200, 142, 218, 262, 315 (in RMB)
Descriptions: Chloroquine phosphate is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. It is an autophagy and toll-like receptor (TLR) inhibitor and is highly effective in controlling SARS-CoV-2 (COVID-19) infection in vitro (EC50 = 1.13 μM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg
Package: A233637
Price: 99, 200, 142, 218, 262, 315 (in RMB)
Descriptions: Chloroquine phosphate is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. It is an autophagy and toll-like receptor (TLR) inhibitor and is highly effective in controlling SARS-CoV-2 (COVID-19) infection in vitro (EC50 = 1.13 μM).
Last Update: 2026-04-17 13:46:08
CAS: 616-91-1
Category: Inhibitors|Agonists, Cell Culture
Spec: 500mg, 1g, 5g, 10g
Package: A233740
Price: 280, 330, 350, 420 (in RMB)
Descriptions: Acetylcysteine is an inhibitor of ROS and the production of TNF. It is a pharmaceutical drug and nutritional supplement used as mucolytic agent.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 500mg, 1g, 5g, 10g
Package: A233740
Price: 280, 330, 350, 420 (in RMB)
Descriptions: Acetylcysteine is an inhibitor of ROS and the production of TNF. It is a pharmaceutical drug and nutritional supplement used as mucolytic agent.
Last Update: 2026-04-17 13:46:08
CAS: 486-16-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 25mg, 50mg, 100mg
Package: A578786
Price: 9540, 12420, 15750 (in RMB)
Descriptions: Carbinoxamine is an antihistamine used to treat allergy symptoms and allergic diseases by blocking histamine H1 receptors to reduce allergic reactions.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 25mg, 50mg, 100mg
Package: A578786
Price: 9540, 12420, 15750 (in RMB)
Descriptions: Carbinoxamine is an antihistamine used to treat allergy symptoms and allergic diseases by blocking histamine H1 receptors to reduce allergic reactions.
Last Update: 2026-04-17 13:46:08
CAS: 1325212-97-2
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A476581
Price: 7560 (in RMB)
Descriptions: GSK2245035 maleate is a selective Toll-like receptor 7 (TLR7) agonist with preferential Type-1 interferon (IFN)-stimulating properties which displays extraordinary IFNα inducing potency and IFNα/TNFα selectivity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A476581
Price: 7560 (in RMB)
Descriptions: GSK2245035 maleate is a selective Toll-like receptor 7 (TLR7) agonist with preferential Type-1 interferon (IFN)-stimulating properties which displays extraordinary IFNα inducing potency and IFNα/TNFα selectivity.
Last Update: 2026-04-17 13:46:08
CAS: 1575591-66-0
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1492852
Price: 532, 798, 1365, 2184, 3500 (in RMB)
Descriptions: Rilzabrutinib is a BTK inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1492852
Price: 532, 798, 1365, 2184, 3500 (in RMB)
Descriptions: Rilzabrutinib is a BTK inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 32602-11-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A218677
Price: 420, 665, 1400, 2240, 3570 (in RMB)
Descriptions: 6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A218677
Price: 420, 665, 1400, 2240, 3570 (in RMB)
Descriptions: 6-Quinoxalinecarboxylic acid, 2, 3-bis (bromomethyl)- is an useful linker for antibody-drug-conjugations (ADCs), extracted from [Bioorg Chem.
Last Update: 2026-04-17 13:46:08
CAS: 5084-19-5
Category: Natural product, Myrtaceae
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1246555
Price: 431, 1292, 2197, 4392, 7467 (in RMB)
Descriptions: Combretol is a natural product isolated from the leaves and roots of Cassipourea madagascariensis, with leishmanicidal activity.
Last Update: 2026-04-17 13:46:08
Category: Natural product, Myrtaceae
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1246555
Price: 431, 1292, 2197, 4392, 7467 (in RMB)
Descriptions: Combretol is a natural product isolated from the leaves and roots of Cassipourea madagascariensis, with leishmanicidal activity.
Last Update: 2026-04-17 13:46:08
CAS: 679809-58-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1216551
Price: 202, 504, 805, 1540, 2380, 3675 (in RMB)
Descriptions: Enoxaparin is one of the most commonly used low-molecular-weight heparins in a wide variety of thromboembolic disorders and has several advantages over unfractionated heparin.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1216551
Price: 202, 504, 805, 1540, 2380, 3675 (in RMB)
Descriptions: Enoxaparin is one of the most commonly used low-molecular-weight heparins in a wide variety of thromboembolic disorders and has several advantages over unfractionated heparin.
Last Update: 2026-04-17 13:46:08
CAS: 103-03-7
Category: Inhibitors|Agonists, Anti-infection
Spec: 5g, 25g, 100g
Package: A989972
Price: 155, 435, 1109 (in RMB)
Descriptions: 1-Phenylsemicarbazide is an antifungal agent with the potential to prevent mold growth in industrial products. It is commonly used for the identification of ketones and aldehydes, reacting with intracellular ketones or aldehydes to impact cellular metabolism.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5g, 25g, 100g
Package: A989972
Price: 155, 435, 1109 (in RMB)
Descriptions: 1-Phenylsemicarbazide is an antifungal agent with the potential to prevent mold growth in industrial products. It is commonly used for the identification of ketones and aldehydes, reacting with intracellular ketones or aldehydes to impact cellular metabolism.
Last Update: 2026-04-17 13:46:08
CAS: 2284621-75-4
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1155022
Price: 429, 945, 1575, 2894, 4725 (in RMB)
Descriptions: JAK/HDAC-IN-1 is a potent JAK2/HDAC dual inhibitor with improved antiproliferative and proapoptotic activities over SAHA and ruxolitinib in several hematological cell lines.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1155022
Price: 429, 945, 1575, 2894, 4725 (in RMB)
Descriptions: JAK/HDAC-IN-1 is a potent JAK2/HDAC dual inhibitor with improved antiproliferative and proapoptotic activities over SAHA and ruxolitinib in several hematological cell lines.
Last Update: 2026-04-17 13:46:08
CAS: 138844-81-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 10mg, 100mg
Package: A612115
Price: 293, 727 (in RMB)
Descriptions: Ibandronate sodium is a highly potent nitrogen-containing bisphosphonate used for the treatment of osteoporosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 10mg, 100mg
Package: A612115
Price: 293, 727 (in RMB)
Descriptions: Ibandronate sodium is a highly potent nitrogen-containing bisphosphonate used for the treatment of osteoporosis.
Last Update: 2026-04-17 13:46:08
CAS: 1309241-34-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1362216
Price: 420, 700, 1190, 1960, 3290, 5600 (in RMB)
Descriptions: GRP-60367 is a potent and selective rabies virus (RABV) entry inhibitor with nanomolar potency against some RABV strains.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1362216
Price: 420, 700, 1190, 1960, 3290, 5600 (in RMB)
Descriptions: GRP-60367 is a potent and selective rabies virus (RABV) entry inhibitor with nanomolar potency against some RABV strains.
Last Update: 2026-04-17 13:46:08
CAS: 202825-45-4
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50mg, 100mg
Package: A423772
Price: 553, 840 (in RMB)
Descriptions: Ralfinamide mesylate is an blocker of Na+ channel with function of suppressing pain.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50mg, 100mg
Package: A423772
Price: 553, 840 (in RMB)
Descriptions: Ralfinamide mesylate is an blocker of Na+ channel with function of suppressing pain.
Last Update: 2026-04-17 13:46:08
CAS: 2628-17-3
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 100mg, 1g
Package: A302673
Price: 221, 693 (in RMB)
Descriptions: 4-Vinylphenol is found in the medicinal herb Hedyotis diffusa Willd, wild rice and is also the metabolite of p-coumaric and ferulic acid by lactic acid bacteria in wine. 4-Vinylphenol induces apoptosis and inhibits blood vessels formation and suppresses invasive breast tumor growth in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 100mg, 1g
Package: A302673
Price: 221, 693 (in RMB)
Descriptions: 4-Vinylphenol is found in the medicinal herb Hedyotis diffusa Willd, wild rice and is also the metabolite of p-coumaric and ferulic acid by lactic acid bacteria in wine. 4-Vinylphenol induces apoptosis and inhibits blood vessels formation and suppresses invasive breast tumor growth in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 1584121-99-2
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg
Package: A1249394
Price: 1002, 2205, 3528 (in RMB)
Descriptions: IT-901 is an orally active inhibitor of the NF-κB subunit c-Rel with good bioactivity, capable of blocking NF-κB and c-Rel DNA binding, suitable for research on human lymphomas and graft-versus-host disease (GVHD).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg
Package: A1249394
Price: 1002, 2205, 3528 (in RMB)
Descriptions: IT-901 is an orally active inhibitor of the NF-κB subunit c-Rel with good bioactivity, capable of blocking NF-κB and c-Rel DNA binding, suitable for research on human lymphomas and graft-versus-host disease (GVHD).
Last Update: 2026-04-17 13:46:08
CAS: 101314-97-0
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A466698
Price: 995 (in RMB)
Descriptions: Simvastatin hydroxy acid sodium is an effective HMG-CoA reductase (HMGCR) inhibitor that significantly reduces indole sulfate-mediated reactive oxygen species (ROS) generation while regulating OATP3A1 expression in cardiomyocytes and OATP3A1-transfected HEK293 cells, demonstrating cardiovascular protective effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A466698
Price: 995 (in RMB)
Descriptions: Simvastatin hydroxy acid sodium is an effective HMG-CoA reductase (HMGCR) inhibitor that significantly reduces indole sulfate-mediated reactive oxygen species (ROS) generation while regulating OATP3A1 expression in cardiomyocytes and OATP3A1-transfected HEK293 cells, demonstrating cardiovascular protective effects.
Last Update: 2026-04-17 13:46:08
CAS: 1307245-87-9
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1001766
Price: 661, 1400, 2442, 4172 (in RMB)
Descriptions: LY-2940094 tartrate is the tartrate form of LY-2940094 which is an antagonist of nociceptin receptor that is used for the treatment of major depressive disorder and alcoholism.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1001766
Price: 661, 1400, 2442, 4172 (in RMB)
Descriptions: LY-2940094 tartrate is the tartrate form of LY-2940094 which is an antagonist of nociceptin receptor that is used for the treatment of major depressive disorder and alcoholism.
Last Update: 2026-04-17 13:46:08
CAS: 58594-72-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 100g, 500g
Package: A361095
Price: 194, 640 (in RMB)
Descriptions: Imazalil sulfate is a fungicide used to protect crops from fungal invasion.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100g, 500g
Package: A361095
Price: 194, 640 (in RMB)
Descriptions: Imazalil sulfate is a fungicide used to protect crops from fungal invasion.
Last Update: 2026-04-17 13:46:08
CAS: 943134-39-2
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A680718
Price: 718, 1725, 2234, 3769, 6030 (in RMB)
Descriptions: GAP-134, a small modified dipeptide, has been identified as a potent and selective second generation gap junction modifier with oral bioavailability.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A680718
Price: 718, 1725, 2234, 3769, 6030 (in RMB)
Descriptions: GAP-134, a small modified dipeptide, has been identified as a potent and selective second generation gap junction modifier with oral bioavailability.
Last Update: 2026-04-17 13:46:08
CAS: 498-95-3
Category: Inhibitors|Agonists, Small Molecule Positive Drug
Spec: 50μL, 1mL, 5g
Package: A278584
Price: 99, 165, 220 (in RMB)
Descriptions: (±)-Nipecotic acid is an inhibitor of GABA uptake with IC50 values of 8, 106 and 2370 mM for hGABA T-1, hGABA T-3 and hBGT-1 respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Small Molecule Positive Drug
Spec: 50μL, 1mL, 5g
Package: A278584
Price: 99, 165, 220 (in RMB)
Descriptions: (±)-Nipecotic acid is an inhibitor of GABA uptake with IC50 values of 8, 106 and 2370 mM for hGABA T-1, hGABA T-3 and hBGT-1 respectively.
Last Update: 2026-04-17 13:46:08
CAS: 202657-55-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1146468
Price: 1680 (in RMB)
Descriptions: Licorice glycoside C2 is an oleanane-type triterpenoid oligosaccharide isolated from Glycyrrhiza uralensis. Licorice extracts exhibit diverse biological activities, including antiviral, antimicrobial, antioxidant, anti-inflammatory, anti-ulcer, anticancer, and anti-HIV effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1146468
Price: 1680 (in RMB)
Descriptions: Licorice glycoside C2 is an oleanane-type triterpenoid oligosaccharide isolated from Glycyrrhiza uralensis. Licorice extracts exhibit diverse biological activities, including antiviral, antimicrobial, antioxidant, anti-inflammatory, anti-ulcer, anticancer, and anti-HIV effects.
Last Update: 2026-04-17 13:46:08
CAS: 634913-39-6
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Package: A1158762
Descriptions: AER-271 is an aquaporin-4 inhibitor which can block the development of early cerebral edema, reduce early neurologic deficit, and blunt neuronal death and neuroinflammation post-cardiac arrest.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Package: A1158762
Descriptions: AER-271 is an aquaporin-4 inhibitor which can block the development of early cerebral edema, reduce early neurologic deficit, and blunt neuronal death and neuroinflammation post-cardiac arrest.
Last Update: 2026-04-17 13:46:08
CAS: 61036-62-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 1g
Package: A417440
Price: 160, 595 (in RMB)
Descriptions: Teicoplanin is a glycopeptide antibiotic used in the prophylaxis and treatment of serious infections caused by Gram-positive bacteria through inhibiting bacterial cell wall synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 1g
Package: A417440
Price: 160, 595 (in RMB)
Descriptions: Teicoplanin is a glycopeptide antibiotic used in the prophylaxis and treatment of serious infections caused by Gram-positive bacteria through inhibiting bacterial cell wall synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 2243944-92-3
Category: Inhibitors|Agonists, Epigenetics
Spec: 1mg, 5mg, 10mg
Package: A1487534
Price: 426, 615, 1228 (in RMB)
Descriptions: FTO-IN-1 is an inhibitor of fat mass and obesity-associated enzyme (FTO) with an IC50 value of less than 1 μM, showing potential for studying obesity-related diseases and cancer, particularly in metabolic and epigenetic regulation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 1mg, 5mg, 10mg
Package: A1487534
Price: 426, 615, 1228 (in RMB)
Descriptions: FTO-IN-1 is an inhibitor of fat mass and obesity-associated enzyme (FTO) with an IC50 value of less than 1 μM, showing potential for studying obesity-related diseases and cancer, particularly in metabolic and epigenetic regulation.
Last Update: 2026-04-17 13:46:08
CAS: 2365478-58-4
Category: Inhibitors|Agonists, Autophagy
Spec: 1mg, 5mg
Package: A1467750
Price: 1655, 3640 (in RMB)
Descriptions: HaloPROTAC-E is a novel HaloPROTAC potent degrader, inducing reversible degradation of two endosomally localized proteins, SGK3 and VPS34, with a DC50 of 3-10 nM, remarkably selective inducing only degradation of the Halo tagged endogenous VPS34 complex (VPS34, VPS15, Beclin1, and ATG14) and no other proteins were significantly degraded.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Autophagy
Spec: 1mg, 5mg
Package: A1467750
Price: 1655, 3640 (in RMB)
Descriptions: HaloPROTAC-E is a novel HaloPROTAC potent degrader, inducing reversible degradation of two endosomally localized proteins, SGK3 and VPS34, with a DC50 of 3-10 nM, remarkably selective inducing only degradation of the Halo tagged endogenous VPS34 complex (VPS34, VPS15, Beclin1, and ATG14) and no other proteins were significantly degraded.
Last Update: 2026-04-17 13:46:08
CAS: 99882-10-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A1378153
Price: 1610 (in RMB)
Descriptions: Kaempferol 3-O-arabinoside is an antioxidant flavonoid isolated from the ethyl acetate fraction (EAF) of Nectandra hihua leaves, exhibiting good antioxidant activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg
Package: A1378153
Price: 1610 (in RMB)
Descriptions: Kaempferol 3-O-arabinoside is an antioxidant flavonoid isolated from the ethyl acetate fraction (EAF) of Nectandra hihua leaves, exhibiting good antioxidant activity.
Last Update: 2026-04-17 13:46:08
CAS: 69698-54-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A725420
Price: 1330, 3360 (in RMB)
Descriptions: VIP(6-28)(human, rat, porcine, bovine) is an effective antagonist of the actions of exogenous vasoactive intestinal peptide (VIP) on cAMP.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A725420
Price: 1330, 3360 (in RMB)
Descriptions: VIP(6-28)(human, rat, porcine, bovine) is an effective antagonist of the actions of exogenous vasoactive intestinal peptide (VIP) on cAMP.
Last Update: 2026-04-17 13:46:08
CAS: 2108567-79-7
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A1443080
Price: 1134, 1764, 3276 (in RMB)
Descriptions: (rel)-ML-SI3 is an isomer of ML-SI3, a TRPML channel inhibitor, blocking TRPML1 and TRPML2 with IC50 values of 4.7 μM and 1.7 μM, respectively, preventing lysosomal calcium efflux and inhibiting TRPML1-mediated autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A1443080
Price: 1134, 1764, 3276 (in RMB)
Descriptions: (rel)-ML-SI3 is an isomer of ML-SI3, a TRPML channel inhibitor, blocking TRPML1 and TRPML2 with IC50 values of 4.7 μM and 1.7 μM, respectively, preventing lysosomal calcium efflux and inhibiting TRPML1-mediated autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 80451-05-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A811939
Price: 910, 2730 (in RMB)
Descriptions: Cecropin B can inhibit the expression of CYP3A29.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A811939
Price: 910, 2730 (in RMB)
Descriptions: Cecropin B can inhibit the expression of CYP3A29.
Last Update: 2026-04-17 13:46:08
CAS: 2984506-77-4
Category: Inhibitors|Agonists, Stem Cells
Spec: 1mg
Package: A1682706
Price: 840 (in RMB)
Descriptions: AK-2292 is an effective selective STAT5 PROTAC degrader with significant biological activity and potential clinical application value.It can specifically degrade STAT5A and STAT5B proteins and has shown potential for treating acute myeloid leukemia (AML) and chronic myeloid leukemia (CML) in in vivo and in vitro studies.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 1mg
Package: A1682706
Price: 840 (in RMB)
Descriptions: AK-2292 is an effective selective STAT5 PROTAC degrader with significant biological activity and potential clinical application value.It can specifically degrade STAT5A and STAT5B proteins and has shown potential for treating acute myeloid leukemia (AML) and chronic myeloid leukemia (CML) in in vivo and in vitro studies.
Last Update: 2026-04-17 13:46:08
CAS: 4135-11-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1250259
Price: 693 (in RMB)
Descriptions: Polymyxin B1 is a lipopeptide antibiotic derived from Paenibacillus polymyxa, which disrupts the integrity of Gram-negative bacteria's outer membrane, leading to cell lysis. This compound is often used to treat multidrug-resistant Gram-negative infections and induces bacterial death by binding to lipopolysaccharides (LPS) in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1250259
Price: 693 (in RMB)
Descriptions: Polymyxin B1 is a lipopeptide antibiotic derived from Paenibacillus polymyxa, which disrupts the integrity of Gram-negative bacteria's outer membrane, leading to cell lysis. This compound is often used to treat multidrug-resistant Gram-negative infections and induces bacterial death by binding to lipopolysaccharides (LPS) in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 1211-19-4
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg
Package: A303109
Price: 109, 385, 197, 315 (in RMB)
Descriptions: SIRT-IN-3 is an effective SIRT inhibitor with an IC50 of 17 μM for SIRT1, and selectivity is 4 times and 14 times for SIRT2 and SIRT3, respectively, making it suitable for SIRT1-mediated metabolism and aging-related research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg
Package: A303109
Price: 109, 385, 197, 315 (in RMB)
Descriptions: SIRT-IN-3 is an effective SIRT inhibitor with an IC50 of 17 μM for SIRT1, and selectivity is 4 times and 14 times for SIRT2 and SIRT3, respectively, making it suitable for SIRT1-mediated metabolism and aging-related research.
Last Update: 2026-04-17 13:46:08
CAS: 1401-69-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172256
Price: 109, 318, 196, 276, 350, 441 (in RMB)
Descriptions: Tylosin is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172256
Price: 109, 318, 196, 276, 350, 441 (in RMB)
Descriptions: Tylosin is a macrolide antibiotic and a bacteriostatic feed additive used in veterinary medicine with a broad spectrum of activity against Gram-positive organisms and a limited range of Gram-negative organisms.
Last Update: 2026-04-17 13:46:08
CAS: 86555-35-3
Category: Inhibitors|Agonists, Epigenetics
Spec: 1mg, 5mg, 10mg
Package: A940358
Price: 504, 981, 1764 (in RMB)
Descriptions: Malantide is a synthetic peptide phosphorylated by PKA and is used to measure PKA activity in vitro.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 1mg, 5mg, 10mg
Package: A940358
Price: 504, 981, 1764 (in RMB)
Descriptions: Malantide is a synthetic peptide phosphorylated by PKA and is used to measure PKA activity in vitro.
Last Update: 2026-04-17 13:46:08
CAS: 2408840-26-4
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 50μL, 1mL, 1mg
Package: A1554635
Price: 169, 946, 350 (in RMB)
Descriptions: Imlunestrant is an orally effective, selective estrogen receptor (ER) degrader (SERD) with pure antagonistic properties. Imlunestrant can persistently inhibit ER-dependent gene transcription and cell growth, suitable for research on ER-positive (ER+) advanced breast cancer (aBC) and endometrial carcinoma (EEC).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 50μL, 1mL, 1mg
Package: A1554635
Price: 169, 946, 350 (in RMB)
Descriptions: Imlunestrant is an orally effective, selective estrogen receptor (ER) degrader (SERD) with pure antagonistic properties. Imlunestrant can persistently inhibit ER-dependent gene transcription and cell growth, suitable for research on ER-positive (ER+) advanced breast cancer (aBC) and endometrial carcinoma (EEC).
Last Update: 2026-04-17 13:46:08
CAS: 2799-07-7
Category: Inhibitors|Agonists, Amino Acid
Spec: 50μL, 1mL, 500mg, 1g
Package: A106724
Price: 109, 385, 1120, 1568 (in RMB)
Descriptions: H-Cys(Trt)-OH is a potent and selective inhibitor of mitotic kinesin Eg5 with IC50 value of 140 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Amino Acid
Spec: 50μL, 1mL, 500mg, 1g
Package: A106724
Price: 109, 385, 1120, 1568 (in RMB)
Descriptions: H-Cys(Trt)-OH is a potent and selective inhibitor of mitotic kinesin Eg5 with IC50 value of 140 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1275595-86-2
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1185078
Price: 859, 1890, 2835, 5930 (in RMB)
Descriptions: Selatinib is a dual EGFR and ErbB2 inhibitor with anticancer activity, capable of inhibiting tumor cell growth. It exhibits oral activity and efficacy, suitable for research on tumor cell growth inhibition.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1185078
Price: 859, 1890, 2835, 5930 (in RMB)
Descriptions: Selatinib is a dual EGFR and ErbB2 inhibitor with anticancer activity, capable of inhibiting tumor cell growth. It exhibits oral activity and efficacy, suitable for research on tumor cell growth inhibition.
Last Update: 2026-04-17 13:46:08
CAS: 324022-39-1
Category: Inhibitors|Agonists, Protease
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1705539
Price: 573, 1260, 2016, 4095 (in RMB)
Descriptions: WNK1-IN-1 is a selective WNK1 kinase inhibitor that regulates ion channels and cellular fluid balance, with potential for treating hypertension and cardiovascular diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Protease
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1705539
Price: 573, 1260, 2016, 4095 (in RMB)
Descriptions: WNK1-IN-1 is a selective WNK1 kinase inhibitor that regulates ion channels and cellular fluid balance, with potential for treating hypertension and cardiovascular diseases.
Last Update: 2026-04-17 13:46:08
CAS: 404844-02-6
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A779949
Price: 498, 1221, 2276, 3541, 5103 (in RMB)
Descriptions: N-Desmethyl imatinib (Norimatinib) is a metabolite of imatinib, a multi-target inhibitor of v-Abl, c-Kit, and PDGFR.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A779949
Price: 498, 1221, 2276, 3541, 5103 (in RMB)
Descriptions: N-Desmethyl imatinib (Norimatinib) is a metabolite of imatinib, a multi-target inhibitor of v-Abl, c-Kit, and PDGFR.
Last Update: 2026-04-17 13:46:08
CAS: 2624131-45-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1533468
Price: 315, 738, 1180, 2110, 3070, 4360 (in RMB)
Descriptions: PW0787 is an orally bioavailable, brain-penetrant, potent, and selective GPR52 agonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1533468
Price: 315, 738, 1180, 2110, 3070, 4360 (in RMB)
Descriptions: PW0787 is an orally bioavailable, brain-penetrant, potent, and selective GPR52 agonist.
Last Update: 2026-04-17 13:46:08
CAS: 1359164-11-6
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A887606
Price: 269, 1706, 601, 1323, 2394, 3150, 4347, 5985 (in RMB)
Descriptions: SR2211 is an effective and selective synthetic modulator of RORγ, acting as an inverse agonist, with a Ki value of 105 nM and an IC50 value of ~320 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A887606
Price: 269, 1706, 601, 1323, 2394, 3150, 4347, 5985 (in RMB)
Descriptions: SR2211 is an effective and selective synthetic modulator of RORγ, acting as an inverse agonist, with a Ki value of 105 nM and an IC50 value of ~320 nM.
Last Update: 2026-04-17 13:46:08
CAS: 36330-85-5
Category: Inhibitors|Agonists, Enzyme Preparation
Spec: 50μL, 1mL, 100mg
Package: A819665
Price: 109, 231, 189 (in RMB)
Descriptions: Fenbufen is a phenylalkanoic derivative with anti-inflammatory, analgesic and antipyretic activity. It is a non-steroidal anti-inflammatory drug.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Enzyme Preparation
Spec: 50μL, 1mL, 100mg
Package: A819665
Price: 109, 231, 189 (in RMB)
Descriptions: Fenbufen is a phenylalkanoic derivative with anti-inflammatory, analgesic and antipyretic activity. It is a non-steroidal anti-inflammatory drug.
Last Update: 2026-04-17 13:46:08
CAS: 1357072-61-7
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A248902
Price: 119, 541, 222, 431, 651, 1959 (in RMB)
Descriptions: c-Met Inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including gastric, glioblastoma, and pancreatic cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A248902
Price: 119, 541, 222, 431, 651, 1959 (in RMB)
Descriptions: c-Met Inhibitor 1 is a c-Met receptor signaling pathway inhibitor, used for the treatment of cancer including gastric, glioblastoma, and pancreatic cancer.
Last Update: 2026-04-17 13:46:08
CAS: 4443-09-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A610417
Price: 491, 1197, 1856 (in RMB)
Descriptions: Norwogonin is a compound isolated from Scutellaria baicalensis, showing activity against enterovirus 71 (EV71) with an IC50 of 31.83 μg/ml. This compound is suitable for antiviral drug development, particularly against enteroviral infections.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A610417
Price: 491, 1197, 1856 (in RMB)
Descriptions: Norwogonin is a compound isolated from Scutellaria baicalensis, showing activity against enterovirus 71 (EV71) with an IC50 of 31.83 μg/ml. This compound is suitable for antiviral drug development, particularly against enteroviral infections.
Last Update: 2026-04-17 13:46:08
CAS: 84-65-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg
Package: A259681
Price: 43 (in RMB)
Descriptions: Anthraquinone is the main active constituents in herbs often used to relieve constipation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg
Package: A259681
Price: 43 (in RMB)
Descriptions: Anthraquinone is the main active constituents in herbs often used to relieve constipation.
Last Update: 2026-04-17 13:46:08
CAS: 2458219-65-1
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg
Package: A1461900
Price: 1400 (in RMB)
Descriptions: SHP2-D26 is a first, potent, and effective PROTAC degrader of SHP2 protein. SHP2-D26 achieves DC50 values of 6.0 and 2.6 nM in esophageal cancer KYSE520 and acute myeloid leukemia MV4;11 cells, respectively, and is capable of reducing SHP2 protein levels by >95% in cancer cells. SHP2-D26 is >30-times more potent in inhibition of phosphorylation of extracellular signal-regulated kinase (ERK) and of cell growth than SHP099, a potent SHP2 inhibitor, in KYSE520 and MV4;11 cancer cell lines.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg
Package: A1461900
Price: 1400 (in RMB)
Descriptions: SHP2-D26 is a first, potent, and effective PROTAC degrader of SHP2 protein. SHP2-D26 achieves DC50 values of 6.0 and 2.6 nM in esophageal cancer KYSE520 and acute myeloid leukemia MV4;11 cells, respectively, and is capable of reducing SHP2 protein levels by >95% in cancer cells. SHP2-D26 is >30-times more potent in inhibition of phosphorylation of extracellular signal-regulated kinase (ERK) and of cell growth than SHP099, a potent SHP2 inhibitor, in KYSE520 and MV4;11 cancer cell lines.
Last Update: 2026-04-17 13:46:08
CAS: 31098-42-7
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg
Package: A1441585
Price: 265, 424 (in RMB)
Descriptions: Amifostine thiol (WR-1065) is the active metabolite of the cell protectant Amifostine. It is a cell protectant with radiation protection capabilities that activate p53 through a JNK-dependent signaling pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg
Package: A1441585
Price: 265, 424 (in RMB)
Descriptions: Amifostine thiol (WR-1065) is the active metabolite of the cell protectant Amifostine. It is a cell protectant with radiation protection capabilities that activate p53 through a JNK-dependent signaling pathway.
Last Update: 2026-04-17 13:46:08
CAS: 159190-44-0
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 5mg, 10mg
Package: A996193
Price: 169, 1089, 624, 1103 (in RMB)
Descriptions: L-NIO dihydrochloride is an effective, non-selective, NADPH-dependent inhibitor of nitric oxide synthase (NOS). It has Ki values of 1.7, 3.9, and 3.9 μM for neuronal (nNOS), endothelial (eNOS), and inducible (iNOS) nitric oxide synthases, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 5mg, 10mg
Package: A996193
Price: 169, 1089, 624, 1103 (in RMB)
Descriptions: L-NIO dihydrochloride is an effective, non-selective, NADPH-dependent inhibitor of nitric oxide synthase (NOS). It has Ki values of 1.7, 3.9, and 3.9 μM for neuronal (nNOS), endothelial (eNOS), and inducible (iNOS) nitric oxide synthases, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 1472795-20-2
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A503888
Price: 109, 469, 140, 400, 560, 1120, 1920, 3200 (in RMB)
Descriptions: KRCA-0008 is a potent and selective ALK/Ack1 inhibitor with IC50 of 12 nM/4 nM for ALK and Ack1 respectively and displays drug-like properties without hERG liability.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A503888
Price: 109, 469, 140, 400, 560, 1120, 1920, 3200 (in RMB)
Descriptions: KRCA-0008 is a potent and selective ALK/Ack1 inhibitor with IC50 of 12 nM/4 nM for ALK and Ack1 respectively and displays drug-like properties without hERG liability.
Last Update: 2026-04-17 13:46:08
CAS: 1164500-72-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1209759
Price: 840, 1400, 2800, 4200 (in RMB)
Descriptions: ML 145 is a selective antagonist of the GPR35 orphan receptor with IC50 of 20.1 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1209759
Price: 840, 1400, 2800, 4200 (in RMB)
Descriptions: ML 145 is a selective antagonist of the GPR35 orphan receptor with IC50 of 20.1 nM.
Last Update: 2026-04-17 13:46:08
CAS: 9005-32-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 100g
Package: A1460321
Price: 150 (in RMB)
Descriptions: Alginic acid is a naturally derived polysaccharide extracted from brown algae, exhibiting excellent biocompatibility and film-forming properties, and is widely used in drug delivery systems and biomaterial research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 100g
Package: A1460321
Price: 150 (in RMB)
Descriptions: Alginic acid is a naturally derived polysaccharide extracted from brown algae, exhibiting excellent biocompatibility and film-forming properties, and is widely used in drug delivery systems and biomaterial research.
Last Update: 2026-04-17 13:46:08
CAS: 537034-15-4
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A889970
Price: 99, 169, 176, 297, 592, 942, 1480 (in RMB)
Descriptions: NKL 22 is a HDAC inhibitor. The value of IC 50 is 78 uM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A889970
Price: 99, 169, 176, 297, 592, 942, 1480 (in RMB)
Descriptions: NKL 22 is a HDAC inhibitor. The value of IC 50 is 78 uM.
Last Update: 2026-04-17 13:46:08
CAS: 37248-47-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg
Package: A668782
Price: 119, 550, 315 (in RMB)
Descriptions: Validamycin A is an agricultural antibiotic fungicide that inhibits the growth of Aspergillus flavus (MIC = 1 μg/mL) and has high inhibition activity against trehalase of Fusarium oxysporum (IC50 = 72 μM). It is also a reversible inhibitor of tyrosinase (Ki = 5.893 mM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg
Package: A668782
Price: 119, 550, 315 (in RMB)
Descriptions: Validamycin A is an agricultural antibiotic fungicide that inhibits the growth of Aspergillus flavus (MIC = 1 μg/mL) and has high inhibition activity against trehalase of Fusarium oxysporum (IC50 = 72 μM). It is also a reversible inhibitor of tyrosinase (Ki = 5.893 mM).
Last Update: 2026-04-17 13:46:08
CAS: 2366268-80-4
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1365063
Price: 2218 (in RMB)
Descriptions: CP-10 is a PROTAC targeting on CDK4/6 with DC50 values of 150-180 nM and 2.1 nM, respectively. It was generated by linking CDK6 inhibitor palbociclib and E3 ligase CRBN recruiter pomalidomide.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1365063
Price: 2218 (in RMB)
Descriptions: CP-10 is a PROTAC targeting on CDK4/6 with DC50 values of 150-180 nM and 2.1 nM, respectively. It was generated by linking CDK6 inhibitor palbociclib and E3 ligase CRBN recruiter pomalidomide.
Last Update: 2026-04-17 13:46:08
CAS: 5652-28-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 10mg, 25mg, 50mg
Package: A874859
Price: 245, 455, 735 (in RMB)
Descriptions: DL-AP3 is a competitive group I metabotropic glutamate receptor antagonist and inhibitor of phosphoserine phosphatase.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 10mg, 25mg, 50mg
Package: A874859
Price: 245, 455, 735 (in RMB)
Descriptions: DL-AP3 is a competitive group I metabotropic glutamate receptor antagonist and inhibitor of phosphoserine phosphatase.
Last Update: 2026-04-17 13:46:08
CAS: 79-14-1
Category: Inhibitors|Agonists, Lipid
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A701706
Price: 109, 350, 120, 145, 175, 210, 252, 315 (in RMB)
Descriptions: Glycolic acid (or hydroxyacetic acid) is the smallest alpha-hydroxy acid. Due to its excellent capability to penetrate skin, glycolic acid is often used in skin care products, most often as a chemical peel.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Lipid
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A701706
Price: 109, 350, 120, 145, 175, 210, 252, 315 (in RMB)
Descriptions: Glycolic acid (or hydroxyacetic acid) is the smallest alpha-hydroxy acid. Due to its excellent capability to penetrate skin, glycolic acid is often used in skin care products, most often as a chemical peel.
Last Update: 2026-04-17 13:46:08
CAS: 203923-89-1
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A236184
Price: 1428, 3570 (in RMB)
Descriptions: BNP 1350 is a topoisomerase I inhibitor, with potent anti-cancer activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A236184
Price: 1428, 3570 (in RMB)
Descriptions: BNP 1350 is a topoisomerase I inhibitor, with potent anti-cancer activity.
Last Update: 2026-04-17 13:46:08
CAS: 143032-85-3
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg
Package: A151425
Price: 1680 (in RMB)
Descriptions: 1alpha-Hydroxy VD4 , a 1alpha (OH)D derivative, can effectively induce the differentiation of monoblastic leukaemia U937, P39/TSU and P31/FUJ cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg
Package: A151425
Price: 1680 (in RMB)
Descriptions: 1alpha-Hydroxy VD4 , a 1alpha (OH)D derivative, can effectively induce the differentiation of monoblastic leukaemia U937, P39/TSU and P31/FUJ cells.
Last Update: 2026-04-17 13:46:08
CAS: 1190389-15-1
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A846150
Price: 1330, 3325 (in RMB)
Descriptions: Vibegron is an effective, selective β3-adrenergic receptor agonist (EC50=1.1 nM) primarily used to treat overactive bladder and severe urgency incontinence, demonstrating significant therapeutic effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A846150
Price: 1330, 3325 (in RMB)
Descriptions: Vibegron is an effective, selective β3-adrenergic receptor agonist (EC50=1.1 nM) primarily used to treat overactive bladder and severe urgency incontinence, demonstrating significant therapeutic effects.
Last Update: 2026-04-17 13:46:08
CAS: 78606-80-1
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A1208573
Price: 1273, 3181 (in RMB)
Descriptions: BML-111 is a lipoxin A4 (LXA4) receptor agonist and a lipoprotein A4 analog. BML-111 demonstrates anti-angiogenic, anti-tumor, and anti-inflammatory properties by inhibiting angiotensin-converting enzyme (ACE) activity and enhancing ACE2 activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A1208573
Price: 1273, 3181 (in RMB)
Descriptions: BML-111 is a lipoxin A4 (LXA4) receptor agonist and a lipoprotein A4 analog. BML-111 demonstrates anti-angiogenic, anti-tumor, and anti-inflammatory properties by inhibiting angiotensin-converting enzyme (ACE) activity and enhancing ACE2 activity.
Last Update: 2026-04-17 13:46:08
CAS: 126453-07-4
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg
Package: A263012
Price: 693 (in RMB)
Descriptions: (R)-CPP is a potent NMDA receptor antagonist widely used in the study of central nervous system diseases, particularly in research on excitotoxicity and neurodegenerative diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg
Package: A263012
Price: 693 (in RMB)
Descriptions: (R)-CPP is a potent NMDA receptor antagonist widely used in the study of central nervous system diseases, particularly in research on excitotoxicity and neurodegenerative diseases.
Last Update: 2026-04-17 13:46:08
CAS: 34450-18-5
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg
Package: A665507
Price: 1015, 1638, 3458 (in RMB)
Descriptions: LTB ω-hydroxylase inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg
Package: A665507
Price: 1015, 1638, 3458 (in RMB)
Descriptions: LTB ω-hydroxylase inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 380449-54-7
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg
Package: A1365946
Price: 1203, 2646 (in RMB)
Descriptions: Melflufen hydrochloride is a dipeptide prodrug of Melphalan, acting as an alkylating agent showing anti-tumor activity against multiple myeloma by irreversibly damaging the DNA of myeloma cells and inducing cytotoxicity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg
Package: A1365946
Price: 1203, 2646 (in RMB)
Descriptions: Melflufen hydrochloride is a dipeptide prodrug of Melphalan, acting as an alkylating agent showing anti-tumor activity against multiple myeloma by irreversibly damaging the DNA of myeloma cells and inducing cytotoxicity.
Last Update: 2026-04-17 13:46:08
CAS: 2004677-13-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1250870
Price: 569, 3773, 1232, 2520, 3780 (in RMB)
Descriptions: Selgantolimod is a Potent and Selective Oral Toll-Like Receptor 8 Agonist for the Treatment of Chronic Hepatitis B.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1250870
Price: 569, 3773, 1232, 2520, 3780 (in RMB)
Descriptions: Selgantolimod is a Potent and Selective Oral Toll-Like Receptor 8 Agonist for the Treatment of Chronic Hepatitis B.
Last Update: 2026-04-17 13:46:08
CAS: 720675-74-1
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1209272
Price: 420, 700, 1400, 2240 (in RMB)
Descriptions: Aryl Hydrocarbon Receptor (AhR) Antagonists, Signal Transduction Modulators
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1209272
Price: 420, 700, 1400, 2240 (in RMB)
Descriptions: Aryl Hydrocarbon Receptor (AhR) Antagonists, Signal Transduction Modulators
Last Update: 2026-04-17 13:46:08
CAS: 1783977-95-6
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg
Package: A1167146
Price: 560, 910, 1925 (in RMB)
Descriptions: XAC is an adenosine receptor antagonist with IC50 value of 16μM for Adenosine Receptor A2.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg
Package: A1167146
Price: 560, 910, 1925 (in RMB)
Descriptions: XAC is an adenosine receptor antagonist with IC50 value of 16μM for Adenosine Receptor A2.
Last Update: 2026-04-17 13:46:08
CAS: 115103-15-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A357500
Price: 378, 630, 1260, 1890, 2835 (in RMB)
Descriptions: Tribendimidine is a broad-spectrum, orally active anthelmintic with particularly high activity against A. lumbricoides and N. americanus. Tribendimidine is also an agonist of L-type nicotinic acetylcholine receptors (nAChR).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A357500
Price: 378, 630, 1260, 1890, 2835 (in RMB)
Descriptions: Tribendimidine is a broad-spectrum, orally active anthelmintic with particularly high activity against A. lumbricoides and N. americanus. Tribendimidine is also an agonist of L-type nicotinic acetylcholine receptors (nAChR).
Last Update: 2026-04-17 13:46:08
CAS: 2306388-65-6
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1544128
Price: 359, 2310, 859, 1890, 3024 (in RMB)
Descriptions: ERRα PROTAC compound I is a highly selective ERRα degradant based on the von Hippel-Lindau ligand, capable of specifically degrading ERRα protein by over 80% at a concentration of 30 nM, with no activity against ERRβ and ERRγ proteins.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1544128
Price: 359, 2310, 859, 1890, 3024 (in RMB)
Descriptions: ERRα PROTAC compound I is a highly selective ERRα degradant based on the von Hippel-Lindau ligand, capable of specifically degrading ERRα protein by over 80% at a concentration of 30 nM, with no activity against ERRβ and ERRγ proteins.
Last Update: 2026-04-17 13:46:08
CAS: 351862-32-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg
Package: A1466897
Price: 299, 1925, 1575, 2394 (in RMB)
Descriptions: Sarizotan (EMD 128130) is an orally active serotonin 5-HT1A receptor and dopamine receptor agonist. Sarizotan (EMD 128130) exhibits IC50 values of 6.5 nM (rat 5-HT1A), 0.1 nM (human 5-HT1A), 15.1 nM (rat D2), 17 nM (human D2), 6.8 nM (human D3) and 2.4 nM (human D4.2), respectively[1].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg
Package: A1466897
Price: 299, 1925, 1575, 2394 (in RMB)
Descriptions: Sarizotan (EMD 128130) is an orally active serotonin 5-HT1A receptor and dopamine receptor agonist. Sarizotan (EMD 128130) exhibits IC50 values of 6.5 nM (rat 5-HT1A), 0.1 nM (human 5-HT1A), 15.1 nM (rat D2), 17 nM (human D2), 6.8 nM (human D3) and 2.4 nM (human D4.2), respectively[1].
Last Update: 2026-04-17 13:46:08
CAS: 1332708-14-1
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A468603
Price: 269, 1796, 630, 1400, 2240 (in RMB)
Descriptions: PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel and elicited TrpA1-mediated nocifensive behaviour in mouse, with EC50 of 97 nM and 23 nM for rTrpA1 and hTrpA1, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A468603
Price: 269, 1796, 630, 1400, 2240 (in RMB)
Descriptions: PF-4840154 is a potent, selective agonist of the rat and human TrpA1 channel and elicited TrpA1-mediated nocifensive behaviour in mouse, with EC50 of 97 nM and 23 nM for rTrpA1 and hTrpA1, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 1291094-73-9
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A237947
Price: 249, 1619, 560, 1470, 2380 (in RMB)
Descriptions: Licogliflozin is a sodium glucose cotransporter (SGLT1 and SGLT2) inhibitor
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A237947
Price: 249, 1619, 560, 1470, 2380 (in RMB)
Descriptions: Licogliflozin is a sodium glucose cotransporter (SGLT1 and SGLT2) inhibitor
Last Update: 2026-04-17 13:46:08
CAS: 2688040-45-9
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A1678567
Price: 249, 1619, 1470, 2310, 3990 (in RMB)
Descriptions: Lirafugratinib hydrochloride is an orally active, irreversible FGFR2 inhibitor effective against FGFR2 mutations and resistant mutations, capable of inducing tumor regression.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A1678567
Price: 249, 1619, 1470, 2310, 3990 (in RMB)
Descriptions: Lirafugratinib hydrochloride is an orally active, irreversible FGFR2 inhibitor effective against FGFR2 mutations and resistant mutations, capable of inducing tumor regression.
Last Update: 2026-04-17 13:46:08
CAS: 2437-29-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg
Package: A1371080
Price: 220 (in RMB)
Descriptions: Malachite green hemioxalate is a triphenylmethane dye used to detect the release of phosphate in enzymatic reactions. It is also an effective and selective inhibitor of IKBKE, inhibiting its downstream targets such as IκBα, p65, and IRF3. Additionally, Malachite green hemioxalate exhibits anticancer activity both in vitro and in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg
Package: A1371080
Price: 220 (in RMB)
Descriptions: Malachite green hemioxalate is a triphenylmethane dye used to detect the release of phosphate in enzymatic reactions. It is also an effective and selective inhibitor of IKBKE, inhibiting its downstream targets such as IκBα, p65, and IRF3. Additionally, Malachite green hemioxalate exhibits anticancer activity both in vitro and in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 1200133-34-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A595198
Price: 179, 1150, 360, 945, 1260, 3780 (in RMB)
Descriptions: VCH-916 is a non-nucleoside inhibitor of HCV NS5B polymerase.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A595198
Price: 179, 1150, 360, 945, 1260, 3780 (in RMB)
Descriptions: VCH-916 is a non-nucleoside inhibitor of HCV NS5B polymerase.
Last Update: 2026-04-17 13:46:08
CAS: 1821143-80-9
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A774966
Price: 129, 699, 225, 630, 1015, 3255 (in RMB)
Descriptions: DMU2139 is a selective inhibitor of CYP1B1 with IC50 of 9 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A774966
Price: 129, 699, 225, 630, 1015, 3255 (in RMB)
Descriptions: DMU2139 is a selective inhibitor of CYP1B1 with IC50 of 9 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1615-02-7
Category: Inhibitors|Agonists, Anti-infection
Spec: 10g, 25g
Package: A204281
Price: 119, 168 (in RMB)
Descriptions: 4-Chlorocinnamic acid inhibits tyrosinase activity and exhibits antibacterial properties, and it also inhibits the growth of Colletotrichum gloeosporioides.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 10g, 25g
Package: A204281
Price: 119, 168 (in RMB)
Descriptions: 4-Chlorocinnamic acid inhibits tyrosinase activity and exhibits antibacterial properties, and it also inhibits the growth of Colletotrichum gloeosporioides.
Last Update: 2026-04-17 13:46:08
CAS: 593-56-6
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1g, 5g
Package: A422985
Price: 126, 175 (in RMB)
Descriptions: Methoxyamine hydrochloride is an orally active and effective inhibitor of base excision repair (BER). It inhibits BER activity by binding to the 3' hydroxyl left after the removal of damaged bases by 3-methylpurine-DNA glycosylase (MPG). Additionally, methoxyamine hydrochloride can directly bind to apurinic (AP) sites. Furthermore, it can synergistically enhance the therapeutic effects of DNA damaging agents.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1g, 5g
Package: A422985
Price: 126, 175 (in RMB)
Descriptions: Methoxyamine hydrochloride is an orally active and effective inhibitor of base excision repair (BER). It inhibits BER activity by binding to the 3' hydroxyl left after the removal of damaged bases by 3-methylpurine-DNA glycosylase (MPG). Additionally, methoxyamine hydrochloride can directly bind to apurinic (AP) sites. Furthermore, it can synergistically enhance the therapeutic effects of DNA damaging agents.
Last Update: 2026-04-17 13:46:08
CAS: 7361-31-1
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 25mg, 50mg, 100mg
Package: A867181
Price: 109, 165, 248 (in RMB)
Descriptions: α-Methyltyrosine methyl ester HCl is a competitive inhibitor of tyrosine hydroxylase, capable of inhibiting the conversion of tyrosine to dopamine and used as a tool in sympathetic nervous system research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 25mg, 50mg, 100mg
Package: A867181
Price: 109, 165, 248 (in RMB)
Descriptions: α-Methyltyrosine methyl ester HCl is a competitive inhibitor of tyrosine hydroxylase, capable of inhibiting the conversion of tyrosine to dopamine and used as a tool in sympathetic nervous system research.
Last Update: 2026-04-17 13:46:08
CAS: 133-08-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g
Package: A244917
Price: 109, 270, 119, 183, 220 (in RMB)
Descriptions: Diethyl butylmalonate exhibits toxicity towards T. pyriformis, with a log(IGC50-1) of 0.557.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g
Package: A244917
Price: 109, 270, 119, 183, 220 (in RMB)
Descriptions: Diethyl butylmalonate exhibits toxicity towards T. pyriformis, with a log(IGC50-1) of 0.557.
Last Update: 2026-04-17 13:46:08
CAS: 946150-57-8
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A922480
Price: 109, 249, 119, 193, 278, 445, 889, 1370, 2260 (in RMB)
Descriptions: Remetinostat, also called SHP-141, is an inhibitor of HDAC with antineoplastic activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A922480
Price: 109, 249, 119, 193, 278, 445, 889, 1370, 2260 (in RMB)
Descriptions: Remetinostat, also called SHP-141, is an inhibitor of HDAC with antineoplastic activity.
Last Update: 2026-04-17 13:46:08
CAS: 5989-54-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 1g
Package: A968589
Price: 109, 385, 215, 738 (in RMB)
Descriptions: (S)-(−)-Limonene, a fragrance monoterpene mainly found in citrus peel oil, is also naturally occurs in the essential oils of herbs, tea tree oil, and turpentine oil.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 1g
Package: A968589
Price: 109, 385, 215, 738 (in RMB)
Descriptions: (S)-(−)-Limonene, a fragrance monoterpene mainly found in citrus peel oil, is also naturally occurs in the essential oils of herbs, tea tree oil, and turpentine oil.
Last Update: 2026-04-17 13:46:08
CAS: 303727-31-3
Category: Inhibitors|Agonists, MAPK|ERK Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A986611
Price: 109, 348, 140, 323, 523, 1090, 1730, 2730 (in RMB)
Descriptions: L-779450 is a potent, ATP-competitive Raf kinase inhibitor (IC50 =10 nM) that displays > 7, > 30 and > 70-fold selectivity over p38α, GSK3β and Lck respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, MAPK|ERK Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A986611
Price: 109, 348, 140, 323, 523, 1090, 1730, 2730 (in RMB)
Descriptions: L-779450 is a potent, ATP-competitive Raf kinase inhibitor (IC50 =10 nM) that displays > 7, > 30 and > 70-fold selectivity over p38α, GSK3β and Lck respectively.
Last Update: 2026-04-17 13:46:08
CAS: 457657-34-0
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A874797
Price: 399, 2657, 791, 2415, 3465 (in RMB)
Descriptions: PA452 is a retinoid X receptor (RXR) antagonist that inhibits the effect of retinoic acid (RA) on Th1/Th2 development.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A874797
Price: 399, 2657, 791, 2415, 3465 (in RMB)
Descriptions: PA452 is a retinoid X receptor (RXR) antagonist that inhibits the effect of retinoic acid (RA) on Th1/Th2 development.
Last Update: 2026-04-17 13:46:08
CAS: 24292-52-2
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 25mg, 1g
Package: A549207
Price: 99, 154, 105, 126 (in RMB)
Descriptions: Hesperidin methylchalcone is a citrus-derived compound with strong antioxidant and anti-inflammatory activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 25mg, 1g
Package: A549207
Price: 99, 154, 105, 126 (in RMB)
Descriptions: Hesperidin methylchalcone is a citrus-derived compound with strong antioxidant and anti-inflammatory activity.
Last Update: 2026-04-17 13:46:08
CAS: 174634-09-4
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A433632
Price: 189, 1210, 315, 693, 1039, 2205, 3276, 5040 (in RMB)
Descriptions: TAS-103 2HCl is a dual inhibitor of topoisomerase-I (topo-I) and topoisomerase-II (topoII).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A433632
Price: 189, 1210, 315, 693, 1039, 2205, 3276, 5040 (in RMB)
Descriptions: TAS-103 2HCl is a dual inhibitor of topoisomerase-I (topo-I) and topoisomerase-II (topoII).
Last Update: 2026-04-17 13:46:08
CAS: 1637300-25-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A935740
Price: 169, 1092, 435, 1134, 1827, 3248 (in RMB)
Descriptions: F64394 is an inverse agonist of GPR3 with pIC50 of 7.3.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A935740
Price: 169, 1092, 435, 1134, 1827, 3248 (in RMB)
Descriptions: F64394 is an inverse agonist of GPR3 with pIC50 of 7.3.
Last Update: 2026-04-17 13:46:08
CAS: 19741-14-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A532297
Price: 134, 209, 435, 699 (in RMB)
Descriptions: Methotrexate metabolite (DAMPA) is an active metabolite of Methotrexate, which is a folate antagonist widely used for immunosuppression.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A532297
Price: 134, 209, 435, 699 (in RMB)
Descriptions: Methotrexate metabolite (DAMPA) is an active metabolite of Methotrexate, which is a folate antagonist widely used for immunosuppression.
Last Update: 2026-04-17 13:46:08
CAS: 714971-87-6
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A594240
Price: 149, 832, 429, 945, 1575, 2660, 3850, 6390 (in RMB)
Descriptions: RO0711401 is an NMDA receptor antagonist that modulates glutamate signaling by blocking NMDA receptors, showing antidepressant and neuroprotective effects by alleviating excitatory neurotransmission in the central nervous system.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A594240
Price: 149, 832, 429, 945, 1575, 2660, 3850, 6390 (in RMB)
Descriptions: RO0711401 is an NMDA receptor antagonist that modulates glutamate signaling by blocking NMDA receptors, showing antidepressant and neuroprotective effects by alleviating excitatory neurotransmission in the central nervous system.
Last Update: 2026-04-17 13:46:08
CAS: 442908-10-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg
Package: A155723
Price: 119, 557, 384, 592, 990, 1970, 2830 (in RMB)
Descriptions: Vipadenant is an adenosine antagonist with Ki of 1.3 nM and 68 nM for A2A and A1, respectively. Vipadenant is a selective A2A receptor antagonist with Ki values of 1.3, 68, 63, and 1,005 nM for A2A, A1, A2B, and A3 receptors, respectively, used in development for for Parkinson's disease.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg
Package: A155723
Price: 119, 557, 384, 592, 990, 1970, 2830 (in RMB)
Descriptions: Vipadenant is an adenosine antagonist with Ki of 1.3 nM and 68 nM for A2A and A1, respectively. Vipadenant is a selective A2A receptor antagonist with Ki values of 1.3, 68, 63, and 1,005 nM for A2A, A1, A2B, and A3 receptors, respectively, used in development for for Parkinson's disease.
Last Update: 2026-04-17 13:46:08
CAS: 792946-69-1
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 50mg, 100mg
Package: A221373
Price: 119, 538, 219, 428, 567, 882, 2457, 3906 (in RMB)
Descriptions: DCLX069 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 value of 17.9 µM, showing significant anticancer activity. It has lower activity against PRMT4 and PRMT6 and is widely used in cancer research, including breast cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 50mg, 100mg
Package: A221373
Price: 119, 538, 219, 428, 567, 882, 2457, 3906 (in RMB)
Descriptions: DCLX069 is a selective protein arginine methyltransferase 1 (PRMT1) inhibitor with an IC50 value of 17.9 µM, showing significant anticancer activity. It has lower activity against PRMT4 and PRMT6 and is widely used in cancer research, including breast cancer.
Last Update: 2026-04-17 13:46:08
CAS: 331830-20-7
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1340294
Price: 109, 462, 378, 598, 1197, 1890, 3087 (in RMB)
Descriptions: 1,4-DPCA is an effective prolyl-4-hydroxylase inhibitor with an IC50 of 2.4 μM that inhibits the degradation of HIF-1α, stabilizing HIF-1α protein while inhibiting FIH (IC50 = 60 μM), suitable for research on hypoxia-related diseases and fibrosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1340294
Price: 109, 462, 378, 598, 1197, 1890, 3087 (in RMB)
Descriptions: 1,4-DPCA is an effective prolyl-4-hydroxylase inhibitor with an IC50 of 2.4 μM that inhibits the degradation of HIF-1α, stabilizing HIF-1α protein while inhibiting FIH (IC50 = 60 μM), suitable for research on hypoxia-related diseases and fibrosis.
Last Update: 2026-04-17 13:46:08
CAS: 652-67-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25g, 50g, 100g, 500g, 1kg
Package: A414539
Price: 99, 154, 100, 140, 200, 400, 560 (in RMB)
Descriptions: Isosorbide is used as a diuretic used mainly to treat hydrocephalus and is also used to treat glaucoma.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25g, 50g, 100g, 500g, 1kg
Package: A414539
Price: 99, 154, 100, 140, 200, 400, 560 (in RMB)
Descriptions: Isosorbide is used as a diuretic used mainly to treat hydrocephalus and is also used to treat glaucoma.
Last Update: 2026-04-17 13:46:08
CAS: 402-71-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A544458
Price: 99, 177, 145, 220, 315 (in RMB)
Descriptions: TPCK is a non-specific irreversible inhibitor of serine/cysteine proteases. It acts by inhibiting ScRce1 in the presence of a Ras reporter, but not in the presence of the a-factor peptide.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A544458
Price: 99, 177, 145, 220, 315 (in RMB)
Descriptions: TPCK is a non-specific irreversible inhibitor of serine/cysteine proteases. It acts by inhibiting ScRce1 in the presence of a Ras reporter, but not in the presence of the a-factor peptide.
Last Update: 2026-04-17 13:46:08
CAS: 91188-00-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1380198
Price: 360, 945, 1575, 3010, 4914 (in RMB)
Descriptions: Merafloxacin is a novel fluoroquinolone antibiotic with significant inhibitory effects against various bacterial infections, applied in infectious disease research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1380198
Price: 360, 945, 1575, 3010, 4914 (in RMB)
Descriptions: Merafloxacin is a novel fluoroquinolone antibiotic with significant inhibitory effects against various bacterial infections, applied in infectious disease research.
Last Update: 2026-04-17 13:46:08
CAS: 1793080-72-4
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1549079
Price: 219, 1439, 686, 1260, 2100, 4200 (in RMB)
Descriptions: VX-150 is a highly selective NaV1.8 inhibitor with oral activity, suitable for research on various pain indications, holding therapeutic potential.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1549079
Price: 219, 1439, 686, 1260, 2100, 4200 (in RMB)
Descriptions: VX-150 is a highly selective NaV1.8 inhibitor with oral activity, suitable for research on various pain indications, holding therapeutic potential.
Last Update: 2026-04-17 13:46:08
CAS: 693241-54-2
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A835001
Price: 208, 517, 833, 1380, 2070, 2890 (in RMB)
Descriptions: EG1 is an inhibitor of Pax2 transcription activation with a small molecule that targets the DNA binding domain.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A835001
Price: 208, 517, 833, 1380, 2070, 2890 (in RMB)
Descriptions: EG1 is an inhibitor of Pax2 transcription activation with a small molecule that targets the DNA binding domain.
Last Update: 2026-04-17 13:46:08
CAS: 1550053-02-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A822432
Price: 149, 891, 258, 567, 907, 1701, 2722, 4082 (in RMB)
Descriptions: BRD3308 is a highly selective inhibitor of histone deacetylase 3 (HDAC3) with an IC50 value of 65 nM for HDAC3 vs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A822432
Price: 149, 891, 258, 567, 907, 1701, 2722, 4082 (in RMB)
Descriptions: BRD3308 is a highly selective inhibitor of histone deacetylase 3 (HDAC3) with an IC50 value of 65 nM for HDAC3 vs.
Last Update: 2026-04-17 13:46:08
CAS: 2244904-70-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1167268
Price: 169, 1078, 445, 668, 980, 1680, 3024, 4536, 6890 (in RMB)
Descriptions: BAY-293 selectively inhibits the KRAS-SOS1 interaction with an IC50 of 21nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1167268
Price: 169, 1078, 445, 668, 980, 1680, 3024, 4536, 6890 (in RMB)
Descriptions: BAY-293 selectively inhibits the KRAS-SOS1 interaction with an IC50 of 21nM.
Last Update: 2026-04-17 13:46:08
CAS: 704888-90-4
Category: Inhibitors|Agonists, Protease
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A443997
Price: 129, 616, 504, 785, 1791, 2740, 3632 (in RMB)
Descriptions: ARP-100 is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Protease
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A443997
Price: 129, 616, 504, 785, 1791, 2740, 3632 (in RMB)
Descriptions: ARP-100 is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM).
Last Update: 2026-04-17 13:46:08
CAS: 302-84-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 100mg, 1g
Package: A125328
Price: 109, 330, 132, 189, 837 (in RMB)
Descriptions: Serine is a non-essential amino acid and a natural ligand and allosteric activator of pyruvate kinase M2.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 100mg, 1g
Package: A125328
Price: 109, 330, 132, 189, 837 (in RMB)
Descriptions: Serine is a non-essential amino acid and a natural ligand and allosteric activator of pyruvate kinase M2.
Last Update: 2026-04-17 13:46:08
CAS: 918505-61-0
Category: Inhibitors|Agonists, MAPK|ERK Pathway
Spec: 5mg, 10mg, 50mg
Package: A364953
Price: 1000, 1600, 4000 (in RMB)
Descriptions: BRAF inhibitor is a potent BRAF inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, MAPK|ERK Pathway
Spec: 5mg, 10mg, 50mg
Package: A364953
Price: 1000, 1600, 4000 (in RMB)
Descriptions: BRAF inhibitor is a potent BRAF inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 1303470-48-5
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg
Package: A299396
Price: 1019, 6756, 2568, 6690 (in RMB)
Descriptions: KHK-IN-1 HCl is a potent ketohexokinase (KHK) inhibitor with IC50 of 12 nM, interacts with Asp-27B in the ATP-binding region of KHK.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg
Package: A299396
Price: 1019, 6756, 2568, 6690 (in RMB)
Descriptions: KHK-IN-1 HCl is a potent ketohexokinase (KHK) inhibitor with IC50 of 12 nM, interacts with Asp-27B in the ATP-binding region of KHK.
Last Update: 2026-04-17 13:46:08
CAS: 2413991-74-7
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50μL, 1mL, 1mg
Package: A1600990
Price: 1289, 8598, 1960 (in RMB)
Descriptions: FT709 is an effective selective USP9X inhibitor with an IC50 of 82 nM, involved in centrosome function, mitotic chromosome alignment, EGF receptor degradation, chemoresistance, and circadian rhythm.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50μL, 1mL, 1mg
Package: A1600990
Price: 1289, 8598, 1960 (in RMB)
Descriptions: FT709 is an effective selective USP9X inhibitor with an IC50 of 82 nM, involved in centrosome function, mitotic chromosome alignment, EGF receptor degradation, chemoresistance, and circadian rhythm.
Last Update: 2026-04-17 13:46:08
CAS: 33649-15-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1482363
Price: 2170 (in RMB)
Descriptions: Tomentosin is a sesquiterpene lactone extracted from Inula helenium, with anti-inflammatory and anticancer activities, capable of inducing apoptosis in pancreatic cancer cells and inhibiting their proliferation, migration, and invasion.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A1482363
Price: 2170 (in RMB)
Descriptions: Tomentosin is a sesquiterpene lactone extracted from Inula helenium, with anti-inflammatory and anticancer activities, capable of inducing apoptosis in pancreatic cancer cells and inhibiting their proliferation, migration, and invasion.
Last Update: 2026-04-17 13:46:08
CAS: 853953-65-8
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1437975
Price: 812, 1458, 1750, 2100, 3360, 5600 (in RMB)
Descriptions: GW604714X is a highly specific MPC (mitochondrial pyruvate carrier) inhibitor with Ki value<0.1nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1437975
Price: 812, 1458, 1750, 2100, 3360, 5600 (in RMB)
Descriptions: GW604714X is a highly specific MPC (mitochondrial pyruvate carrier) inhibitor with Ki value<0.1nM.
Last Update: 2026-04-17 13:46:08
CAS: 486-39-5
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg
Package: A232032
Price: 630, 1610 (in RMB)
Descriptions: Coclaurine, a natural product isolated and purified from the root of Coptis chinensis Franch, blocks postsynaptic but not presynaptic dopamine receptors in the mouse striatum.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg
Package: A232032
Price: 630, 1610 (in RMB)
Descriptions: Coclaurine, a natural product isolated and purified from the root of Coptis chinensis Franch, blocks postsynaptic but not presynaptic dopamine receptors in the mouse striatum.
Last Update: 2026-04-17 13:46:08
CAS: 53155-25-2
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A848633
Price: 630, 1750, 2590 (in RMB)
Descriptions: Euscaphic acid, a natural product isolated and purified from the dried fruit of Ziziphus jujuba, with anti-diabetic and anti-inflammatory activities, induces death by activation of caspase-3, dependent apoptotic pathway, and inhibits LPS-induced inflammatory responses by interference with the clustering of TRAF6 with IRAK1 and TAK1, resulting in blocking the activation of IKK and MAPKs signal transduction to downregulate NF-κB activations.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A848633
Price: 630, 1750, 2590 (in RMB)
Descriptions: Euscaphic acid, a natural product isolated and purified from the dried fruit of Ziziphus jujuba, with anti-diabetic and anti-inflammatory activities, induces death by activation of caspase-3, dependent apoptotic pathway, and inhibits LPS-induced inflammatory responses by interference with the clustering of TRAF6 with IRAK1 and TAK1, resulting in blocking the activation of IKK and MAPKs signal transduction to downregulate NF-κB activations.
Last Update: 2026-04-17 13:46:08
CAS: 2163793-38-0
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg
Package: A1339690
Price: 583, 1631 (in RMB)
Descriptions: PROTAC Mcl1 degrader-1 (compound C3) is a PROTAC targeting on Bcl-2 and Mcl-1 with DC50 values of 3μM and 0.7μM, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg
Package: A1339690
Price: 583, 1631 (in RMB)
Descriptions: PROTAC Mcl1 degrader-1 (compound C3) is a PROTAC targeting on Bcl-2 and Mcl-1 with DC50 values of 3μM and 0.7μM, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 299420-83-0
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A870662
Price: 535, 1260, 2142 (in RMB)
Descriptions: UC-514321 is a structural analog of NSC370284 with higher activity, targeting STAT3/5 and selectively inhibiting the expression of TET1. It exhibits good anti-acute myeloid leukemia activity both in vitro and in vivo with low toxicity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A870662
Price: 535, 1260, 2142 (in RMB)
Descriptions: UC-514321 is a structural analog of NSC370284 with higher activity, targeting STAT3/5 and selectively inhibiting the expression of TET1. It exhibits good anti-acute myeloid leukemia activity both in vitro and in vivo with low toxicity.
Last Update: 2026-04-17 13:46:08
CAS: 123940-54-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A948115
Price: 559, 1120, 1680 (in RMB)
Descriptions: Hypocrellin B, a natural product isolated and purified from Hypocrella bambusae, has sonodynamic action to induce mitochondrial damage, survival inhibition, apoptosis and inhibit adhesion and migration of cancer cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A948115
Price: 559, 1120, 1680 (in RMB)
Descriptions: Hypocrellin B, a natural product isolated and purified from Hypocrella bambusae, has sonodynamic action to induce mitochondrial damage, survival inhibition, apoptosis and inhibit adhesion and migration of cancer cells.
Last Update: 2026-04-17 13:46:08
CAS: 69640-38-6
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 50μL, 1mL, 1mg, 5mg
Package: A1553747
Price: 489, 3234, 1197, 2646 (in RMB)
Descriptions: Pentachloropseudilin is a reversible myosin inhibitor with an IC50 of 1-5 μM against class I myosin, effectively inhibiting TGF-β-induced signaling.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 50μL, 1mL, 1mg, 5mg
Package: A1553747
Price: 489, 3234, 1197, 2646 (in RMB)
Descriptions: Pentachloropseudilin is a reversible myosin inhibitor with an IC50 of 1-5 μM against class I myosin, effectively inhibiting TGF-β-induced signaling.
Last Update: 2026-04-17 13:46:08
CAS: 1794760-28-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 2mg, 5mg, 10mg
Package: A1329790
Price: 443, 665, 1155, 1715 (in RMB)
Descriptions: PD-144418 Oxalate is a novel selective sigma ligand.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 2mg, 5mg, 10mg
Package: A1329790
Price: 443, 665, 1155, 1715 (in RMB)
Descriptions: PD-144418 Oxalate is a novel selective sigma ligand.
Last Update: 2026-04-17 13:46:08
CAS: 1314873-02-3
Category: Inhibitors|Agonists, Autophagy
Spec: 1mg, 5mg, 10mg
Package: A725109
Price: 361, 1112, 1567 (in RMB)
Descriptions: BPO-27 racemate is an effective CFTR inhibitor with an IC50 of 8 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Autophagy
Spec: 1mg, 5mg, 10mg
Package: A725109
Price: 361, 1112, 1567 (in RMB)
Descriptions: BPO-27 racemate is an effective CFTR inhibitor with an IC50 of 8 nM.
Last Update: 2026-04-17 13:46:08
CAS: 70351-51-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1209933
Price: 378, 832, 1285, 2646, 4385 (in RMB)
Descriptions: Supercinnamaldehyde is a potent transient receptor potential ankyrin 1 (TRPA1) activator with an EC50 of 0.8 μM. Its mechanism involves covalent modification of cysteine residues, leading to TRPA1 ion channel activation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1209933
Price: 378, 832, 1285, 2646, 4385 (in RMB)
Descriptions: Supercinnamaldehyde is a potent transient receptor potential ankyrin 1 (TRPA1) activator with an EC50 of 0.8 μM. Its mechanism involves covalent modification of cysteine residues, leading to TRPA1 ion channel activation.
Last Update: 2026-04-17 13:46:08
CAS: 2543545-44-2
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549679
Price: 339, 2229, 723, 2023, 3360 (in RMB)
Descriptions: LT052 is a highly selective BET BD1 inhibitor with an IC50 of 87.7 nM, exhibiting nanomolar-level inhibition of BRD4 BD1, with 138 times selectivity over BRD4 BD2 (IC50 = 12.130 μM). LT052 exhibits anti-inflammatory activity and can be used for acute gouty arthritis research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549679
Price: 339, 2229, 723, 2023, 3360 (in RMB)
Descriptions: LT052 is a highly selective BET BD1 inhibitor with an IC50 of 87.7 nM, exhibiting nanomolar-level inhibition of BRD4 BD1, with 138 times selectivity over BRD4 BD2 (IC50 = 12.130 μM). LT052 exhibits anti-inflammatory activity and can be used for acute gouty arthritis research.
Last Update: 2026-04-17 13:46:08
CAS: 432531-71-0
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1191953
Price: 287, 486, 826, 1400 (in RMB)
Descriptions: Necrosulfonamide is a necroptosis inhibitor by blocking mixed lineage kinase domain-like protein (MLKL), a key substrate of receptor-interacting serine-threonine kinase 3 (RIP3).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1191953
Price: 287, 486, 826, 1400 (in RMB)
Descriptions: Necrosulfonamide is a necroptosis inhibitor by blocking mixed lineage kinase domain-like protein (MLKL), a key substrate of receptor-interacting serine-threonine kinase 3 (RIP3).
Last Update: 2026-04-17 13:46:08
CAS: 1478364-68-9
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1169679
Price: 320, 840, 1330, 2800, 4095 (in RMB)
Descriptions: PXS-4728A (BI-1467335) is an orally active and selective semicarbazide-sensitive amine oxidase (SSAO) inhibitor that improves chronic obstructive pulmonary disease (COPD) in mice.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1169679
Price: 320, 840, 1330, 2800, 4095 (in RMB)
Descriptions: PXS-4728A (BI-1467335) is an orally active and selective semicarbazide-sensitive amine oxidase (SSAO) inhibitor that improves chronic obstructive pulmonary disease (COPD) in mice.
Last Update: 2026-04-17 13:46:08
CAS: 1675201-90-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1210509
Price: 275, 693, 1134, 2100, 3220 (in RMB)
Descriptions: BMS-8 is a compound that inhibits the PD-1/PD-L1 interaction, with an IC50 of 7.2 μM. It binds directly to PD-L1, inducing the formation of PD-L1 homodimers, thus preventing its binding to PD-1.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1210509
Price: 275, 693, 1134, 2100, 3220 (in RMB)
Descriptions: BMS-8 is a compound that inhibits the PD-1/PD-L1 interaction, with an IC50 of 7.2 μM. It binds directly to PD-L1, inducing the formation of PD-L1 homodimers, thus preventing its binding to PD-1.
Last Update: 2026-04-17 13:46:08
CAS: 1287761-01-6
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1258087
Price: 279, 1842, 630, 1540, 2450, 3402, 4083, 4900 (in RMB)
Descriptions: PTUPB is a novel dual COX2 and sHE (soluble epoxide hydrolase) inhibitor. Treatment with PTUPB reduced body weight, liver weight, liver triglyceride and cholesterol content, and the expression of lipolytic/lipogenic and lipid uptake related genes (Acc, Cd36, and Cidec) in HFD mice. This made it be a promising potential therapy for liver steatosis associated with obesity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1258087
Price: 279, 1842, 630, 1540, 2450, 3402, 4083, 4900 (in RMB)
Descriptions: PTUPB is a novel dual COX2 and sHE (soluble epoxide hydrolase) inhibitor. Treatment with PTUPB reduced body weight, liver weight, liver triglyceride and cholesterol content, and the expression of lipolytic/lipogenic and lipid uptake related genes (Acc, Cd36, and Cidec) in HFD mice. This made it be a promising potential therapy for liver steatosis associated with obesity.
Last Update: 2026-04-17 13:46:08
CAS: 16290-26-9
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 100mg
Package: A399015
Price: 250 (in RMB)
Descriptions: 3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) is an improved dopamine analog cytotoxic and inhibits DNA polymerase activity in melanoma cells. 3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) displays growth inhibitory activity in melanoma cell lines with varying degrees of tyrosinase activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 100mg
Package: A399015
Price: 250 (in RMB)
Descriptions: 3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) is an improved dopamine analog cytotoxic and inhibits DNA polymerase activity in melanoma cells. 3,4-Dihydroxybenzylamine hydrobromide (NSC 263475 hydrobromide) displays growth inhibitory activity in melanoma cell lines with varying degrees of tyrosinase activity.
Last Update: 2026-04-17 13:46:08
CAS: 93565-01-6
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A147556
Price: 252, 630, 1008, 1862, 2800, 4200 (in RMB)
Descriptions: MDL 72527 HCl is a polyamine oxidase (PAO) inhibitor with neuroprotective effects. It prevents the production of H2O2 by inhibiting polyamine oxidase, thereby increasing cell viability.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A147556
Price: 252, 630, 1008, 1862, 2800, 4200 (in RMB)
Descriptions: MDL 72527 HCl is a polyamine oxidase (PAO) inhibitor with neuroprotective effects. It prevents the production of H2O2 by inhibiting polyamine oxidase, thereby increasing cell viability.
Last Update: 2026-04-17 13:46:08
CAS: 1897-45-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 250mg, 500mg, 1g
Package: A337418
Price: 220, 276, 398 (in RMB)
Descriptions: Chlorothalonil is a broad-spectrum foliar fungicide with oral activity, used to control fungal diseases on vegetables and crops. It alters the microbial community in soil, inhibits spermatogenesis, induces intestinal epithelial barrier dysfunction, and causes embryotoxicity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 250mg, 500mg, 1g
Package: A337418
Price: 220, 276, 398 (in RMB)
Descriptions: Chlorothalonil is a broad-spectrum foliar fungicide with oral activity, used to control fungal diseases on vegetables and crops. It alters the microbial community in soil, inhibits spermatogenesis, induces intestinal epithelial barrier dysfunction, and causes embryotoxicity.
Last Update: 2026-04-17 13:46:08
CAS: 880813-36-5
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1109706
Price: 169, 918, 315, 693, 1109, 2016, 3024, 4253 (in RMB)
Descriptions: PhiKan 083 is a carbazole derivative that stabilizes the p53 mutant Y220C, with a Kd value of 167 μM. PhiKan 083 can be used in cancer research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1109706
Price: 169, 918, 315, 693, 1109, 2016, 3024, 4253 (in RMB)
Descriptions: PhiKan 083 is a carbazole derivative that stabilizes the p53 mutant Y220C, with a Kd value of 167 μM. PhiKan 083 can be used in cancer research.
Last Update: 2026-04-17 13:46:08
CAS: 1130067-34-3
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A382489
Price: 169, 914, 479, 969, 1568, 2654, 3851, 5392 (in RMB)
Descriptions: CAY10594 is a selective PLD2 inhibitor with IC50 values of 140nM and 5.1μM for PLD2 and PLD1, respectively. It strongly inhibits the invasive migration of breast cancer cells in transwell assays.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A382489
Price: 169, 914, 479, 969, 1568, 2654, 3851, 5392 (in RMB)
Descriptions: CAY10594 is a selective PLD2 inhibitor with IC50 values of 140nM and 5.1μM for PLD2 and PLD1, respectively. It strongly inhibits the invasive migration of breast cancer cells in transwell assays.
Last Update: 2026-04-17 13:46:08
CAS: 13080-21-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg, 100mg, 250mg
Package: A314292
Price: 167, 279, 833, 1180, 2571 (in RMB)
Descriptions: HPi1 is a potent, selective, and orally active antimicrobial agent targeting Helicobacter pylori, with no activity against other bacteria, including Lactobacillus species.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg, 100mg, 250mg
Package: A314292
Price: 167, 279, 833, 1180, 2571 (in RMB)
Descriptions: HPi1 is a potent, selective, and orally active antimicrobial agent targeting Helicobacter pylori, with no activity against other bacteria, including Lactobacillus species.
Last Update: 2026-04-17 13:46:08
CAS: 478-08-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A602082
Price: 169, 1079, 361, 665, 1155, 2713, 3842 (in RMB)
Descriptions: Lucidin is a natural component of Rubia tinctorum L.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A602082
Price: 169, 1079, 361, 665, 1155, 2713, 3842 (in RMB)
Descriptions: Lucidin is a natural component of Rubia tinctorum L.
Last Update: 2026-04-17 13:46:08
CAS: 1118-68-9
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 500mg, 5g
Package: A314013
Price: 109, 330, 189, 252 (in RMB)
Descriptions: N,N-Dimethylglycine, a natural N-methylated glycine, can be as an antioxidant and used to synthesize variety of biochemical drugs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 500mg, 5g
Package: A314013
Price: 109, 330, 189, 252 (in RMB)
Descriptions: N,N-Dimethylglycine, a natural N-methylated glycine, can be as an antioxidant and used to synthesize variety of biochemical drugs.
Last Update: 2026-04-17 13:46:08
CAS: 461000-66-8
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1209836
Price: 119, 594, 567, 787, 1575, 2425, 3402 (in RMB)
Descriptions: Eact is an activator of TMEM16A calcium-activated chloride channel (CaCC) with EC50 of 3 μM. It is also transient receptor potential vanilloid 1 (TRPV1) channel activator (EC50 = 11.6 μM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1209836
Price: 119, 594, 567, 787, 1575, 2425, 3402 (in RMB)
Descriptions: Eact is an activator of TMEM16A calcium-activated chloride channel (CaCC) with EC50 of 3 μM. It is also transient receptor potential vanilloid 1 (TRPV1) channel activator (EC50 = 11.6 μM).
Last Update: 2026-04-17 13:46:08
CAS: 2708934-53-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1523532
Price: 149, 804, 825, 1427, 3002, 4130 (in RMB)
Descriptions: CCF0058981 is a ML300-derived, non-covalent SARS-CoV‑2 3CLpro inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1523532
Price: 149, 804, 825, 1427, 3002, 4130 (in RMB)
Descriptions: CCF0058981 is a ML300-derived, non-covalent SARS-CoV‑2 3CLpro inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 69004-04-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A603396
Price: 109, 427, 216, 346, 761, 914 (in RMB)
Descriptions: Toltrazuril sulfone (Ponazuril) is a metabolite of Toltrazuril with antiprotozoal activity. It is a triazine-class anticoccidial agent developed for the prevention of poultry coccidiosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A603396
Price: 109, 427, 216, 346, 761, 914 (in RMB)
Descriptions: Toltrazuril sulfone (Ponazuril) is a metabolite of Toltrazuril with antiprotozoal activity. It is a triazine-class anticoccidial agent developed for the prevention of poultry coccidiosis.
Last Update: 2026-04-17 13:46:08
CAS: 117-37-3
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 25mg, 100mg, 500mg
Package: A970855
Price: 109, 270, 183, 280, 560 (in RMB)
Descriptions: Anisindione is a synthetic anticoagulant, prevents the formation of active procoagulation factors II, VII, IX, and X.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 25mg, 100mg, 500mg
Package: A970855
Price: 109, 270, 183, 280, 560 (in RMB)
Descriptions: Anisindione is a synthetic anticoagulant, prevents the formation of active procoagulation factors II, VII, IX, and X.
Last Update: 2026-04-17 13:46:08
CAS: 10040-45-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 50mg, 100mg
Package: A345614
Price: 80, 100, 112, 352, 580 (in RMB)
Descriptions: Sodium Picosulfate is used to treat constipation or induce colon cleansing to prepare the large bowels before colonoscopy or surgery.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 50mg, 100mg
Package: A345614
Price: 80, 100, 112, 352, 580 (in RMB)
Descriptions: Sodium Picosulfate is used to treat constipation or induce colon cleansing to prepare the large bowels before colonoscopy or surgery.
Last Update: 2026-04-17 13:46:08
CAS: 2826-26-8
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A630950
Price: 99, 152, 139, 209, 382, 518, 699 (in RMB)
Descriptions: Tyrphostin A1 inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A630950
Price: 99, 152, 139, 209, 382, 518, 699 (in RMB)
Descriptions: Tyrphostin A1 inhibits CD40L-stimulated IL-12 production in macrophage cultures and antigen-induced generation of Th1 cells.
Last Update: 2026-04-17 13:46:08
CAS: 74209-34-0
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A114732
Price: 99, 158, 126, 175, 497, 802 (in RMB)
Descriptions: 3-Bromo-7-nitroindazole is a more potent and selective inhibitor of neuronal nitric oxide synthase (nNOS) than eNOS or inducible nitric oxide synthase (iNOS). 3-Bromo-7-nitroindazole affects the intercellular messenger nitric oxide (NO) synthesis throughout the body and brain.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A114732
Price: 99, 158, 126, 175, 497, 802 (in RMB)
Descriptions: 3-Bromo-7-nitroindazole is a more potent and selective inhibitor of neuronal nitric oxide synthase (nNOS) than eNOS or inducible nitric oxide synthase (iNOS). 3-Bromo-7-nitroindazole affects the intercellular messenger nitric oxide (NO) synthesis throughout the body and brain.
Last Update: 2026-04-17 13:46:08
CAS: 66246-88-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg
Package: A198278
Price: 109, 385, 280, 504 (in RMB)
Descriptions: Penconazole is a triazole fungicide used mainly to control powdery mildew in apples, grapes, and vegetables. It acts by inhibiting fungal sterol biosynthes is and also reduces acetylcholinesterase (AChE) activity in the brains and cerebella of rats.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg
Package: A198278
Price: 109, 385, 280, 504 (in RMB)
Descriptions: Penconazole is a triazole fungicide used mainly to control powdery mildew in apples, grapes, and vegetables. It acts by inhibiting fungal sterol biosynthes is and also reduces acetylcholinesterase (AChE) activity in the brains and cerebella of rats.
Last Update: 2026-04-17 13:46:08
CAS: 2162962-69-6
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A155468
Price: 109, 435, 315, 787, 1254, 2069, 2897, 4055 (in RMB)
Descriptions: CU-CPT9a is a selective Toll-like receptor 8 (TLR8) inhibitor with IC50 of 0.5 nM. It can also suppress TNF-α levels.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A155468
Price: 109, 435, 315, 787, 1254, 2069, 2897, 4055 (in RMB)
Descriptions: CU-CPT9a is a selective Toll-like receptor 8 (TLR8) inhibitor with IC50 of 0.5 nM. It can also suppress TNF-α levels.
Last Update: 2026-04-17 13:46:08
CAS: 3820-67-5
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 100mg, 250mg, 500mg, 1g
Package: A124438
Price: 109, 462, 378, 630, 1134, 1434 (in RMB)
Descriptions: Glafenine is a non-steroidal anti-inflammatory drug (NSAID), is a non-narcotic analgesic agent, widely used for the treatment of pains of various origins.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 100mg, 250mg, 500mg, 1g
Package: A124438
Price: 109, 462, 378, 630, 1134, 1434 (in RMB)
Descriptions: Glafenine is a non-steroidal anti-inflammatory drug (NSAID), is a non-narcotic analgesic agent, widely used for the treatment of pains of various origins.
Last Update: 2026-04-17 13:46:08
CAS: 78954-23-1
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1349796
Price: 290, 725, 1134, 2268, 3654 (in RMB)
Descriptions: Yakuchinone A, derived from Alpinia oxyphylla, has pro-apoptotic activity and shows promising prospects in cancer and anti-inflammatory research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1349796
Price: 290, 725, 1134, 2268, 3654 (in RMB)
Descriptions: Yakuchinone A, derived from Alpinia oxyphylla, has pro-apoptotic activity and shows promising prospects in cancer and anti-inflammatory research.
Last Update: 2026-04-17 13:46:08
CAS: 2767422-72-8
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1680479
Price: 504, 1134, 1764, 3465, 5544 (in RMB)
Descriptions: HS-276 is a TAK1 inhibitor that regulates immune responses by interfering with TAK1 kinase activity. It has application prospects in rheumatoid arthritis and inflammation research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1680479
Price: 504, 1134, 1764, 3465, 5544 (in RMB)
Descriptions: HS-276 is a TAK1 inhibitor that regulates immune responses by interfering with TAK1 kinase activity. It has application prospects in rheumatoid arthritis and inflammation research.
Last Update: 2026-04-17 13:46:08
CAS: 10161-87-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1527471
Price: 119, 501, 450, 770, 1624, 2761 (in RMB)
Descriptions: KRA-533 is a kind of KRAS agonist. By binding to GTP/GDP binding bag in KRAS protein, it prevents the cleavage of GTP, thus leading to the accumulation of constitutive active GTP binding to KRAS, thus activating downstream signal pathways, such as ERK, caspase3 and PARP cleavage, and finally leading to apoptosis and autophagy, showing strong anti-tumor activity in KRAS mutant lung cancer model.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1527471
Price: 119, 501, 450, 770, 1624, 2761 (in RMB)
Descriptions: KRA-533 is a kind of KRAS agonist. By binding to GTP/GDP binding bag in KRAS protein, it prevents the cleavage of GTP, thus leading to the accumulation of constitutive active GTP binding to KRAS, thus activating downstream signal pathways, such as ERK, caspase3 and PARP cleavage, and finally leading to apoptosis and autophagy, showing strong anti-tumor activity in KRAS mutant lung cancer model.
Last Update: 2026-04-17 13:46:08
CAS: 38821-49-7
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A788203
Price: 163, 227, 393, 488, 678 (in RMB)
Descriptions: Carbidopa Monohydrate is a decarboxylase inhibitor, can be used in combination with levodopa for treatment of Parkinsonism.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A788203
Price: 163, 227, 393, 488, 678 (in RMB)
Descriptions: Carbidopa Monohydrate is a decarboxylase inhibitor, can be used in combination with levodopa for treatment of Parkinsonism.
Last Update: 2026-04-17 13:46:08
CAS: 791835-21-7
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1173077
Price: 209, 1309, 504, 1260, 1785, 4998 (in RMB)
Descriptions: BI-6C9 is a Bid inhibitor, which prevents mitochondrial outer membrane potential (MOMP) and mitochondrial fission, and protects the cells from cell death.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1173077
Price: 209, 1309, 504, 1260, 1785, 4998 (in RMB)
Descriptions: BI-6C9 is a Bid inhibitor, which prevents mitochondrial outer membrane potential (MOMP) and mitochondrial fission, and protects the cells from cell death.
Last Update: 2026-04-17 13:46:08
CAS: 259674-19-6
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1176853
Price: 129, 693, 567, 945, 1785, 2646, 3990 (in RMB)
Descriptions: TRPM8 antagonist 14 is a tryptophan-derived selective TRPM8 antagonist with IC50 value of 0.2nM. It showed significant target coverage in both an icilin-induced WDS (at 1-30 mg/kg s.c.) and oxaliplatin-induced cold allodynia (at 0.1-1 μg s.c.) mice models.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1176853
Price: 129, 693, 567, 945, 1785, 2646, 3990 (in RMB)
Descriptions: TRPM8 antagonist 14 is a tryptophan-derived selective TRPM8 antagonist with IC50 value of 0.2nM. It showed significant target coverage in both an icilin-induced WDS (at 1-30 mg/kg s.c.) and oxaliplatin-induced cold allodynia (at 0.1-1 μg s.c.) mice models.
Last Update: 2026-04-17 13:46:08
CAS: 346640-08-2
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A754516
Price: 119, 578, 164, 252, 472, 693, 1449, 2394, 3654 (in RMB)
Descriptions: CCF642 is a PDI-inhibiting compound with antimyeloma activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A754516
Price: 119, 578, 164, 252, 472, 693, 1449, 2394, 3654 (in RMB)
Descriptions: CCF642 is a PDI-inhibiting compound with antimyeloma activity.
Last Update: 2026-04-17 13:46:08
CAS: 1225278-16-9
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A181353
Price: 129, 669, 283, 622, 1110, 2464, 3941, 5875 (in RMB)
Descriptions: DCC-2618 is a c-Kit and PDGFR inhibitor with IC50s of 6/30/13 nM for c-Kit/PDGFRα/PDGFRβ respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A181353
Price: 129, 669, 283, 622, 1110, 2464, 3941, 5875 (in RMB)
Descriptions: DCC-2618 is a c-Kit and PDGFR inhibitor with IC50s of 6/30/13 nM for c-Kit/PDGFRα/PDGFRβ respectively.
Last Update: 2026-04-17 13:46:08
CAS: 897657-95-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A912137
Price: 119, 539, 441, 630, 2100, 3150 (in RMB)
Descriptions: MSX-122 is an orally available partial antagonist of CXCR4, inhibiting CXCR4/CXCL12 interaction with an IC50 of approximately 10 nM. MSX-122 exhibits anti-inflammatory and anti-metastatic activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A912137
Price: 119, 539, 441, 630, 2100, 3150 (in RMB)
Descriptions: MSX-122 is an orally available partial antagonist of CXCR4, inhibiting CXCR4/CXCL12 interaction with an IC50 of approximately 10 nM. MSX-122 exhibits anti-inflammatory and anti-metastatic activities.
Last Update: 2026-04-17 13:46:08
CAS: 878419-78-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A299036
Price: 119, 519, 212, 497, 738, 1190, 1780, 2470 (in RMB)
Descriptions: Walrycin B is an antibacterial compound specifically targeting the essential WalR response regulator.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A299036
Price: 119, 519, 212, 497, 738, 1190, 1780, 2470 (in RMB)
Descriptions: Walrycin B is an antibacterial compound specifically targeting the essential WalR response regulator.
Last Update: 2026-04-17 13:46:08
CAS: 802906-73-6
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A467450
Price: 109, 497, 284, 693, 1112, 2057, 3264 (in RMB)
Descriptions: RG7090 is a potent, selective and orally available mGlu5 negative allosteric modulator with a Kd of 1.1 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A467450
Price: 109, 497, 284, 693, 1112, 2057, 3264 (in RMB)
Descriptions: RG7090 is a potent, selective and orally available mGlu5 negative allosteric modulator with a Kd of 1.1 nM.
Last Update: 2026-04-17 13:46:08
CAS: 62013-04-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 250mg, 500mg, 1g
Package: A612277
Price: 80, 100, 196, 224, 336 (in RMB)
Descriptions: Dirithromycin is a semi-synthetic macrolide antibiotic pro-drug used to treat many different types of bacterial infections, such as bronchitis, pneumonia, tonsillitis, and even skin infections.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 250mg, 500mg, 1g
Package: A612277
Price: 80, 100, 196, 224, 336 (in RMB)
Descriptions: Dirithromycin is a semi-synthetic macrolide antibiotic pro-drug used to treat many different types of bacterial infections, such as bronchitis, pneumonia, tonsillitis, and even skin infections.
Last Update: 2026-04-17 13:46:08
CAS: 1233948-35-0
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A814378
Price: 109, 209, 253, 350, 630, 1050, 1733 (in RMB)
Descriptions: ELR510444 is an inhibitor of tubulin polymerization with IC50 value of 10 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A814378
Price: 109, 209, 253, 350, 630, 1050, 1733 (in RMB)
Descriptions: ELR510444 is an inhibitor of tubulin polymerization with IC50 value of 10 μM.
Last Update: 2026-04-17 13:46:08
CAS: 1259028-99-3
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1154444
Price: 945, 1575, 3150, 5040 (in RMB)
Descriptions: BTT-3033 is an orally active, conformation-selective α2β1 inhibitor (EC50: 130 nM) that binds to the α2I domain. BTT-3033 inhibits platelet binding to collagen I and cell proliferation, and induces apoptosis. BTT-3033 can be used for research in prostate cancer, inflammation, and cardiovascular diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1154444
Price: 945, 1575, 3150, 5040 (in RMB)
Descriptions: BTT-3033 is an orally active, conformation-selective α2β1 inhibitor (EC50: 130 nM) that binds to the α2I domain. BTT-3033 inhibits platelet binding to collagen I and cell proliferation, and induces apoptosis. BTT-3033 can be used for research in prostate cancer, inflammation, and cardiovascular diseases.
Last Update: 2026-04-17 13:46:08
CAS: 353512-04-6
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1364451
Price: 109, 233, 315, 535, 850, 1512, 2205, 3276 (in RMB)
Descriptions: JAK2-IN-6 is an effective selective JAK2 inhibitor, with an IC50 of 22.86 μg/mL. It lacks activity against JAK1 and JAK3 but exhibits anti-proliferative effects against cancer cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1364451
Price: 109, 233, 315, 535, 850, 1512, 2205, 3276 (in RMB)
Descriptions: JAK2-IN-6 is an effective selective JAK2 inhibitor, with an IC50 of 22.86 μg/mL. It lacks activity against JAK1 and JAK3 but exhibits anti-proliferative effects against cancer cells.
Last Update: 2026-04-17 13:46:08
CAS: 1182-34-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A572864
Price: 560, 2240, 3500 (in RMB)
Descriptions: Cynarin comes from the flowerbud of Lonicera japonica Thunb. It has antioxidant property and inhibites HIV-1 replication in MT-2 cell culture at non-toxic concentrations, a potent and highly selective class of HIV-1 integrase inhibitors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A572864
Price: 560, 2240, 3500 (in RMB)
Descriptions: Cynarin comes from the flowerbud of Lonicera japonica Thunb. It has antioxidant property and inhibites HIV-1 replication in MT-2 cell culture at non-toxic concentrations, a potent and highly selective class of HIV-1 integrase inhibitors.
Last Update: 2026-04-17 13:46:08
CAS: 106577-39-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A999814
Price: 350, 1050, 1540 (in RMB)
Descriptions: Hederacolchiside A1 is a compound isolated from Coptis chinensis that induces apoptosis in tumor cells by regulating the PI3K/Akt/mTOR signaling pathway, inhibiting tumor cell proliferation. This compound also shows antischistosomal activity, affecting parasite survival both in vitro and in vivo, suitable for anti-tumor and anti-parasitic research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A999814
Price: 350, 1050, 1540 (in RMB)
Descriptions: Hederacolchiside A1 is a compound isolated from Coptis chinensis that induces apoptosis in tumor cells by regulating the PI3K/Akt/mTOR signaling pathway, inhibiting tumor cell proliferation. This compound also shows antischistosomal activity, affecting parasite survival both in vitro and in vivo, suitable for anti-tumor and anti-parasitic research.
Last Update: 2026-04-17 13:46:08
CAS: 187724-61-4
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1210157
Price: 179, 1155, 347, 738, 1110, 1980, 2980 (in RMB)
Descriptions: PKI-166 is an efficient, selective, orally active EGFR tyrosine kinase inhibitor with an IC50 value of 0.7 nM. This compound is widely used in research on EGFR-dependent cancers, particularly in non-small cell lung cancer and breast cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1210157
Price: 179, 1155, 347, 738, 1110, 1980, 2980 (in RMB)
Descriptions: PKI-166 is an efficient, selective, orally active EGFR tyrosine kinase inhibitor with an IC50 value of 0.7 nM. This compound is widely used in research on EGFR-dependent cancers, particularly in non-small cell lung cancer and breast cancer.
Last Update: 2026-04-17 13:46:08
CAS: 5534-95-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A459112
Price: 346, 504, 1008, 1638, 2772 (in RMB)
Descriptions: Pentagastrin (ICI-50123) is a selective agonist of Cholecystokinin B (CCKB) receptor with an IC50 of 11 nM. Pentagastrin is a synthetic polypeptide that has effects like gastrin when given parenterally, which can cause the secretion and synthesis of salivary proteins.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A459112
Price: 346, 504, 1008, 1638, 2772 (in RMB)
Descriptions: Pentagastrin (ICI-50123) is a selective agonist of Cholecystokinin B (CCKB) receptor with an IC50 of 11 nM. Pentagastrin is a synthetic polypeptide that has effects like gastrin when given parenterally, which can cause the secretion and synthesis of salivary proteins.
Last Update: 2026-04-17 13:46:08
CAS: 32502-62-8
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1005353
Price: 169, 903, 396, 931, 1400, 3227 (in RMB)
Descriptions: 3-Methyltoxoflavin is a potent Protein disulfide isomerase (PDI) inhibitor, with an IC50 of 170 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1005353
Price: 169, 903, 396, 931, 1400, 3227 (in RMB)
Descriptions: 3-Methyltoxoflavin is a potent Protein disulfide isomerase (PDI) inhibitor, with an IC50 of 170 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1215721-40-6
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 50mg
Package: A621191
Price: 169, 990, 188, 298, 447, 1910 (in RMB)
Descriptions: CP-809101 HCl is a potent and selective 5-HT2C receptor agonist with pEC50 of 9.96/7.19/6.81 for human 5-HT2C/5-HT2B/5-HT2A receptors respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 50mg
Package: A621191
Price: 169, 990, 188, 298, 447, 1910 (in RMB)
Descriptions: CP-809101 HCl is a potent and selective 5-HT2C receptor agonist with pEC50 of 9.96/7.19/6.81 for human 5-HT2C/5-HT2B/5-HT2A receptors respectively.
Last Update: 2026-04-17 13:46:08
CAS: 129029-23-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A367930
Price: 139, 713, 265, 693, 945, 1723, 2625, 3850 (in RMB)
Descriptions: Ocaperidone is a benzisoxazole is an antagonist of both 5HT and D2 receptors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A367930
Price: 139, 713, 265, 693, 945, 1723, 2625, 3850 (in RMB)
Descriptions: Ocaperidone is a benzisoxazole is an antagonist of both 5HT and D2 receptors.
Last Update: 2026-04-17 13:46:08
CAS: 2355377-13-6
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1493606
Price: 139, 704, 261, 646, 1129, 1925, 2792 (in RMB)
Descriptions: DDO-5936 is an effective and specific inhibitor of the Hsp90-Cdc37 protein interaction, useful for colon cancer research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1493606
Price: 139, 704, 261, 646, 1129, 1925, 2792 (in RMB)
Descriptions: DDO-5936 is an effective and specific inhibitor of the Hsp90-Cdc37 protein interaction, useful for colon cancer research.
Last Update: 2026-04-17 13:46:08
CAS: 908115-27-5
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A210227
Price: 139, 721, 453, 567, 756, 1638, 2457, 3780 (in RMB)
Descriptions: PF-04929113 is a potent and selective HSP90 inhibitor with Kd of 41 nM and induces Her-2 degradation with IC50 of 37 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A210227
Price: 139, 721, 453, 567, 756, 1638, 2457, 3780 (in RMB)
Descriptions: PF-04929113 is a potent and selective HSP90 inhibitor with Kd of 41 nM and induces Her-2 degradation with IC50 of 37 nM.
Last Update: 2026-04-17 13:46:08
CAS: 781652-57-1
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A231672
Price: 119, 561, 286, 630, 1008, 3024, 4210 (in RMB)
Descriptions: CDPPB is a potent, selective and brain penetrant positive allosteric modulator of the metabotropic glutamate receptor subtype 5 (mGluR5), with an EC50 of 27 nM in Chinese hamster ovary cells expressing human mGluR5.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A231672
Price: 119, 561, 286, 630, 1008, 3024, 4210 (in RMB)
Descriptions: CDPPB is a potent, selective and brain penetrant positive allosteric modulator of the metabotropic glutamate receptor subtype 5 (mGluR5), with an EC50 of 27 nM in Chinese hamster ovary cells expressing human mGluR5.
Last Update: 2026-04-17 13:46:08
CAS: 932737-65-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A723977
Price: 109, 412, 315, 504, 756, 1512, 2268, 3339 (in RMB)
Descriptions: FITM is a negative allosteric modulator of mGlu1 receptor with a Ki of 2.5 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A723977
Price: 109, 412, 315, 504, 756, 1512, 2268, 3339 (in RMB)
Descriptions: FITM is a negative allosteric modulator of mGlu1 receptor with a Ki of 2.5 nM.
Last Update: 2026-04-17 13:46:08
CAS: 76748-86-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A790526
Price: 109, 424, 346, 485, 976, 1669 (in RMB)
Descriptions: Pyronaridine tetraphosphate is an orally active antimalarial drug effective against Plasmodium falciparum and Echinococcus granulosus infections, with notable anti-infective activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A790526
Price: 109, 424, 346, 485, 976, 1669 (in RMB)
Descriptions: Pyronaridine tetraphosphate is an orally active antimalarial drug effective against Plasmodium falciparum and Echinococcus granulosus infections, with notable anti-infective activity.
Last Update: 2026-04-17 13:46:08
CAS: 1672684-68-2
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1177083
Price: 109, 379, 123, 343, 480, 980, 1575, 2352 (in RMB)
Descriptions: MS402 is a domain-selective inhibitor of BRD4-BD1 with Ki value of 77nM, over BRD4-BD2.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1177083
Price: 109, 379, 123, 343, 480, 980, 1575, 2352 (in RMB)
Descriptions: MS402 is a domain-selective inhibitor of BRD4-BD1 with Ki value of 77nM, over BRD4-BD2.
Last Update: 2026-04-17 13:46:08
CAS: 74611-28-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A774432
Price: 109, 280, 731, 1238, 2115, 3589, 6109 (in RMB)
Descriptions: Methiothepin mesylate is a potent and non-selective 5-HT2 receptor antagonist, with pKds of 7.10 (5-HT1A), 7.28 (5HT1B), 7.56 (5HT1C), 6.99 (5HT1D), 7.0 (5-HT5A), 7.8 (5-HT5B), 8.74 (5-HT6), and 8.99 (5-HT7), and pKis of 8.50 (5HT2A), 8.68 (5HT2B), and 8.35 (5HT2C).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A774432
Price: 109, 280, 731, 1238, 2115, 3589, 6109 (in RMB)
Descriptions: Methiothepin mesylate is a potent and non-selective 5-HT2 receptor antagonist, with pKds of 7.10 (5-HT1A), 7.28 (5HT1B), 7.56 (5HT1C), 6.99 (5HT1D), 7.0 (5-HT5A), 7.8 (5-HT5B), 8.74 (5-HT6), and 8.99 (5-HT7), and pKis of 8.50 (5HT2A), 8.68 (5HT2B), and 8.35 (5HT2C).
Last Update: 2026-04-17 13:46:08
CAS: 3505-38-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 25mg, 100mg, 500mg
Package: A242556
Price: 80, 100, 147, 336, 910 (in RMB)
Descriptions: Carbinoxamine maleate is a blocker of histamine-H1 receptor with antihistamine and anticholinergic effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 25mg, 100mg, 500mg
Package: A242556
Price: 80, 100, 147, 336, 910 (in RMB)
Descriptions: Carbinoxamine maleate is a blocker of histamine-H1 receptor with antihistamine and anticholinergic effects.
Last Update: 2026-04-17 13:46:08
CAS: 1702816-75-8
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A724078
Price: 219, 1450, 479, 1008, 1543, 2954, 4890 (in RMB)
Descriptions: Linperlisib (YY-20394) is an effective orally active, selectively PI3Kδ inhibitor with an IC50 of 6.4 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A724078
Price: 219, 1450, 479, 1008, 1543, 2954, 4890 (in RMB)
Descriptions: Linperlisib (YY-20394) is an effective orally active, selectively PI3Kδ inhibitor with an IC50 of 6.4 nM.
Last Update: 2026-04-17 13:46:08
CAS: 108238-41-1
Category: Inhibitors|Agonists, Endoplasmic reticulum stress
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A975493
Price: 109, 385, 70, 104, 311, 462 (in RMB)
Descriptions: 3,6-Dihydroxyflavone is a flavonoid with anticancer activity, inducing apoptosis through activation of caspase cascades and cleavage of poly(ADP-ribose) polymerase (PARP), while increasing intracellular oxidative stress and lipid peroxidation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Endoplasmic reticulum stress
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A975493
Price: 109, 385, 70, 104, 311, 462 (in RMB)
Descriptions: 3,6-Dihydroxyflavone is a flavonoid with anticancer activity, inducing apoptosis through activation of caspase cascades and cleavage of poly(ADP-ribose) polymerase (PARP), while increasing intracellular oxidative stress and lipid peroxidation.
Last Update: 2026-04-17 13:46:08
CAS: 1314533-27-1
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A287827
Price: 392, 840, 1330, 2660, 3955 (in RMB)
Descriptions: Azemiglitazone potassium (MSDC-0602K) is a thiazolidinedione compound that binds to PPARγ (IC50 = 18.25 μM) while modulating mitochondrial pyruvate carriers (MPC). It is used in research on fatty liver disease and its associated lipid metabolism disorders, inflammation, and insulin resistance. As an insulin sensitizer, Azemiglitazone potassium, alone or in combination with Liraglutide, improves hyperinsulinemia and fatty liver disease in mice.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A287827
Price: 392, 840, 1330, 2660, 3955 (in RMB)
Descriptions: Azemiglitazone potassium (MSDC-0602K) is a thiazolidinedione compound that binds to PPARγ (IC50 = 18.25 μM) while modulating mitochondrial pyruvate carriers (MPC). It is used in research on fatty liver disease and its associated lipid metabolism disorders, inflammation, and insulin resistance. As an insulin sensitizer, Azemiglitazone potassium, alone or in combination with Liraglutide, improves hyperinsulinemia and fatty liver disease in mice.
Last Update: 2026-04-17 13:46:08
CAS: 2733573-94-7
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg
Package: A2630708
Price: 4095 (in RMB)
Descriptions: RLY-2608 is the first selective allosteric inhibitor of PI3Kα, exhibiting high specificity and potent anticancer activity, making it suitable for research on PI3Kα mutation-driven cancers and showing promising preclinical potential.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg
Package: A2630708
Price: 4095 (in RMB)
Descriptions: RLY-2608 is the first selective allosteric inhibitor of PI3Kα, exhibiting high specificity and potent anticancer activity, making it suitable for research on PI3Kα mutation-driven cancers and showing promising preclinical potential.
Last Update: 2026-04-17 13:46:08
CAS: 1181226-02-7
Category: Inhibitors|Agonists, Neuronal Signaling
Package: A301812
Descriptions: ZL006 is a potent inhibitor of nNOS/PSD-95 interaction, and inhibits NMDA receptor-mediated NO synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Package: A301812
Descriptions: ZL006 is a potent inhibitor of nNOS/PSD-95 interaction, and inhibits NMDA receptor-mediated NO synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 2378801-85-3
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg
Package: A1216749
Price: 3850 (in RMB)
Descriptions: PROTAC Bcl2 degrader-1 (Compound C5) is a PROTAC targeting on Bcl-2 and Mcl-1 with DC50 values of 3μM and 0.7μM, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg
Package: A1216749
Price: 3850 (in RMB)
Descriptions: PROTAC Bcl2 degrader-1 (Compound C5) is a PROTAC targeting on Bcl-2 and Mcl-1 with DC50 values of 3μM and 0.7μM, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 603987-59-3
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50mg
Package: A447852
Price: 3675 (in RMB)
Descriptions: TY-51469 is a chymase inhibitor with IC50s for simian and human chymases of 0.4 and 7.0 nM, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50mg
Package: A447852
Price: 3675 (in RMB)
Descriptions: TY-51469 is a chymase inhibitor with IC50s for simian and human chymases of 0.4 and 7.0 nM, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 117230-33-8
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A458127
Price: 2520 (in RMB)
Descriptions: Soyasaponin Aa is a soy saponin that exerts anti-obesity effects in 3T3-L1 adipocytes by downregulating PPARγ.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A458127
Price: 2520 (in RMB)
Descriptions: Soyasaponin Aa is a soy saponin that exerts anti-obesity effects in 3T3-L1 adipocytes by downregulating PPARγ.
Last Update: 2026-04-17 13:46:08
CAS: 2509359-75-3
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1467727
Price: 2940 (in RMB)
Descriptions: CP5V is a PROTAC targeting on Cdc20 with DC50 value of 1.6μM, comprising a Cdc20 ligand and VHL binding moiety bridged by a PEG5 linker. It leads to significant inhibition of breast cancer cell proliferation and resensitization of Taxol-resistant cell lines and suppressed breast tumor progression in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1467727
Price: 2940 (in RMB)
Descriptions: CP5V is a PROTAC targeting on Cdc20 with DC50 value of 1.6μM, comprising a Cdc20 ligand and VHL binding moiety bridged by a PEG5 linker. It leads to significant inhibition of breast cancer cell proliferation and resensitization of Taxol-resistant cell lines and suppressed breast tumor progression in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 7184-60-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A966535
Price: 2130 (in RMB)
Descriptions: Borrelidin (also known as Treponemycin) is a macrolide antibiotic that inhibits threonyl-tRNA synthetase, exhibits potent anti-angiogenic effects, induces endothelial cell apoptosis, and shows resistance to malaria.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A966535
Price: 2130 (in RMB)
Descriptions: Borrelidin (also known as Treponemycin) is a macrolide antibiotic that inhibits threonyl-tRNA synthetase, exhibits potent anti-angiogenic effects, induces endothelial cell apoptosis, and shows resistance to malaria.
Last Update: 2026-04-17 13:46:08
CAS: 2055741-39-2
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1550589
Price: 2240 (in RMB)
Descriptions: IV-361 is an orally effective and selective CDK7 inhibitor (Ki ≤ 50 nM) with antitumor activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A1550589
Price: 2240 (in RMB)
Descriptions: IV-361 is an orally effective and selective CDK7 inhibitor (Ki ≤ 50 nM) with antitumor activity.
Last Update: 2026-04-17 13:46:08
CAS: 53584-43-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg
Package: A1365328
Price: 2019, 13482, 4508 (in RMB)
Descriptions: 5-Galloylquinic acid is the main ROS scavenger in green tea.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg
Package: A1365328
Price: 2019, 13482, 4508 (in RMB)
Descriptions: 5-Galloylquinic acid is the main ROS scavenger in green tea.
Last Update: 2026-04-17 13:46:08
CAS: 932359-76-7
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg, 5mg
Package: A1603996
Price: 2013, 5570 (in RMB)
Descriptions: FiVe1 is an effective vimentin (VIM) inhibitor, where VIM is an intermediate filament and mesenchymal marker. FiVe1 promotes VIM degradation and phosphorylation during metaphase, leading to mitotic abnormalities, multinucleation, and loss of stemness. Additionally, FiVe1 selectively and irreversibly inhibits the proliferation of multiple FOXC2-expressing breast cancer cell lines (IC50: 267 nM for HMLER cells; IC50: 447 nM for FOXC2-HMLER cells) and suppresses the migration of mesenchymal transition cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg, 5mg
Package: A1603996
Price: 2013, 5570 (in RMB)
Descriptions: FiVe1 is an effective vimentin (VIM) inhibitor, where VIM is an intermediate filament and mesenchymal marker. FiVe1 promotes VIM degradation and phosphorylation during metaphase, leading to mitotic abnormalities, multinucleation, and loss of stemness. Additionally, FiVe1 selectively and irreversibly inhibits the proliferation of multiple FOXC2-expressing breast cancer cell lines (IC50: 267 nM for HMLER cells; IC50: 447 nM for FOXC2-HMLER cells) and suppresses the migration of mesenchymal transition cells.
Last Update: 2026-04-17 13:46:08
CAS: 91683-38-4
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A171446
Price: 1764 (in RMB)
Descriptions: Gemfibrozil 1-O-β-Glucuronide, a metabolite of Gemfibrozil (CI-719; HY-B0258), is a potent and competitive P450 (CYP) isoform CYP2C8 inhibitor with an IC50 of 4.07 μM[1][2].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg
Package: A171446
Price: 1764 (in RMB)
Descriptions: Gemfibrozil 1-O-β-Glucuronide, a metabolite of Gemfibrozil (CI-719; HY-B0258), is a potent and competitive P450 (CYP) isoform CYP2C8 inhibitor with an IC50 of 4.07 μM[1][2].
Last Update: 2026-04-17 13:46:08
CAS: 864741-95-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A822692
Price: 1898, 4835, 7250 (in RMB)
Descriptions: SB 699551 is a selective 5-ht5a receptor antagonist (pKi values are 8.3, < 6.0, < 6.0, < 6.0, < 5.5 and < 5.5 for 5-ht5a, 5-HT1B/D, 5-HT2A, 5-HT2C, 5-HT1A and 5-HT7 receptors respectively).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A822692
Price: 1898, 4835, 7250 (in RMB)
Descriptions: SB 699551 is a selective 5-ht5a receptor antagonist (pKi values are 8.3, < 6.0, < 6.0, < 6.0, < 5.5 and < 5.5 for 5-ht5a, 5-HT1B/D, 5-HT2A, 5-HT2C, 5-HT1A and 5-HT7 receptors respectively).
Last Update: 2026-04-17 13:46:08
CAS: 5092-09-1
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A474583
Price: 1750, 4200 (in RMB)
Descriptions: Saikogenin A, extracted from a Chinese herbal plant called Tsai-Fu, is a dipeptidyl peptidase-IV (DPP-IV) inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A474583
Price: 1750, 4200 (in RMB)
Descriptions: Saikogenin A, extracted from a Chinese herbal plant called Tsai-Fu, is a dipeptidyl peptidase-IV (DPP-IV) inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 3026986-17-1
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A2432839
Price: 1681, 4203 (in RMB)
Descriptions: SJ3149 is a selective degrader of CK1α (Casein Kinase 1 Alpha), demonstrating significant in vitro and in vivo antitumor activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A2432839
Price: 1681, 4203 (in RMB)
Descriptions: SJ3149 is a selective degrader of CK1α (Casein Kinase 1 Alpha), demonstrating significant in vitro and in vivo antitumor activity.
Last Update: 2026-04-17 13:46:08
CAS: 67884-12-2
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A115890
Price: 1600, 4500 (in RMB)
Descriptions: Martynoside, a natural product isolated and purified from the herbs of Plantago asiatica L., has antioxidative, anticancer and antimetastatic activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A115890
Price: 1600, 4500 (in RMB)
Descriptions: Martynoside, a natural product isolated and purified from the herbs of Plantago asiatica L., has antioxidative, anticancer and antimetastatic activities.
Last Update: 2026-04-17 13:46:08
CAS: 1633824-78-8
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg
Package: A1673454
Price: 1575, 3862 (in RMB)
Descriptions: Elobixibat hydrate is an effective inhibitor of the bile acid transporter (IBAT), with IC50 values of 0.53±0.17 nM (human IBAT), 0.13±0.03 nM (mouse IBAT), and 5.8±1.6 nM (canine IBAT). Elobixibat hydrate can be used in research on chronic idiopathic constipation (CIC) in the elderly.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg
Package: A1673454
Price: 1575, 3862 (in RMB)
Descriptions: Elobixibat hydrate is an effective inhibitor of the bile acid transporter (IBAT), with IC50 values of 0.53±0.17 nM (human IBAT), 0.13±0.03 nM (mouse IBAT), and 5.8±1.6 nM (canine IBAT). Elobixibat hydrate can be used in research on chronic idiopathic constipation (CIC) in the elderly.
Last Update: 2026-04-17 13:46:08
CAS: 36062-07-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 25mg, 50mg
Package: A797477
Price: 1550, 3800, 5500 (in RMB)
Descriptions: Octahydrocurcumin is a hydrogenated derivatives of curcumin and a metabolite of curcumin.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 25mg, 50mg
Package: A797477
Price: 1550, 3800, 5500 (in RMB)
Descriptions: Octahydrocurcumin is a hydrogenated derivatives of curcumin and a metabolite of curcumin.
Last Update: 2026-04-17 13:46:08
CAS: 274675-25-1
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg
Package: A492603
Price: 1512, 3780 (in RMB)
Descriptions: Xanthohumol D, a natural product isolated and purified from the herbs of Humulus lupulus, is a potent inhibitor of quinone reductase-2 (QR-2) with IC50 of 110μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg
Package: A492603
Price: 1512, 3780 (in RMB)
Descriptions: Xanthohumol D, a natural product isolated and purified from the herbs of Humulus lupulus, is a potent inhibitor of quinone reductase-2 (QR-2) with IC50 of 110μM.
Last Update: 2026-04-17 13:46:08
CAS: 27003-73-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A209865
Price: 1323 (in RMB)
Descriptions: Lariciresinol, a natural product isolated and purified from the herbs of Phyllanthus niruri, possesses fungicidal activities by disrupting the fungal plasma membrane. (-)-Lariciresinol and its 7S,8S,8'R stereoisomer can inhibit the root growth of Italian ryegrass to 51-55% relative to the negative control.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg
Package: A209865
Price: 1323 (in RMB)
Descriptions: Lariciresinol, a natural product isolated and purified from the herbs of Phyllanthus niruri, possesses fungicidal activities by disrupting the fungal plasma membrane. (-)-Lariciresinol and its 7S,8S,8'R stereoisomer can inhibit the root growth of Italian ryegrass to 51-55% relative to the negative control.
Last Update: 2026-04-17 13:46:08
CAS: 173792-61-5
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg
Package: A1144642
Price: 1290, 2980 (in RMB)
Descriptions: Kudinoside D is the main triterpene saponin from Ilex kudingcha, which can inhibit fat accumulation in 3T3-L1 adipocytes by regulating the AMPK pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg
Package: A1144642
Price: 1290, 2980 (in RMB)
Descriptions: Kudinoside D is the main triterpene saponin from Ilex kudingcha, which can inhibit fat accumulation in 3T3-L1 adipocytes by regulating the AMPK pathway.
Last Update: 2026-04-17 13:46:08
CAS: 791828-58-5
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A938154
Price: 1273, 2800 (in RMB)
Descriptions: Aderbasib is a sheddase inhibitor, is also an orally bioavailable inhibitor of the ADAM (A disintegrin and metalloprotease) family of multifunctional membrane-bound proteins with potential antineoplastic activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg
Package: A938154
Price: 1273, 2800 (in RMB)
Descriptions: Aderbasib is a sheddase inhibitor, is also an orally bioavailable inhibitor of the ADAM (A disintegrin and metalloprotease) family of multifunctional membrane-bound proteins with potential antineoplastic activity.
Last Update: 2026-04-17 13:46:08
CAS: 378746-64-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1440611
Price: 1232, 2604 (in RMB)
Descriptions: Nemonoxacin is an orally available non-fluorinated quinolone antibiotic with broad-spectrum antibacterial activity, effectively inhibiting Staphylococcus, Streptococcus, Enterococcus, Neisseria gonorrhoeae, and Haemophilus influenzae, and is used in the study of bacterial infections and community-acquired pneumonia.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1440611
Price: 1232, 2604 (in RMB)
Descriptions: Nemonoxacin is an orally available non-fluorinated quinolone antibiotic with broad-spectrum antibacterial activity, effectively inhibiting Staphylococcus, Streptococcus, Enterococcus, Neisseria gonorrhoeae, and Haemophilus influenzae, and is used in the study of bacterial infections and community-acquired pneumonia.
Last Update: 2026-04-17 13:46:08
CAS: 2922824-09-5
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg
Package: A2421879
Price: 1184, 1858 (in RMB)
Descriptions: GPX4-IN-5 is a covalent inhibitor of GPX4, with an IC50 of 0.12 μM, capable of inducing ferroptosis and used in research on triple-negative breast cancer (TNBC).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg
Package: A2421879
Price: 1184, 1858 (in RMB)
Descriptions: GPX4-IN-5 is a covalent inhibitor of GPX4, with an IC50 of 0.12 μM, capable of inducing ferroptosis and used in research on triple-negative breast cancer (TNBC).
Last Update: 2026-04-17 13:46:08
CAS: 203192-01-2
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg
Package: A1251823
Price: 1166, 1400, 2100 (in RMB)
Descriptions: MN58b is a CHKα inhibitor that inhibits phosphocholine synthesis and reduced cell growth through induction of apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg
Package: A1251823
Price: 1166, 1400, 2100 (in RMB)
Descriptions: MN58b is a CHKα inhibitor that inhibits phosphocholine synthesis and reduced cell growth through induction of apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 19833-12-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1146098
Price: 1180, 2930 (in RMB)
Descriptions: Myricetin 3-O-glucoside is a flavonol extracted from Tibouchina paratropica, with activities against Leishmania, anti-inflammatory, and antimicrobial properties.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1146098
Price: 1180, 2930 (in RMB)
Descriptions: Myricetin 3-O-glucoside is a flavonol extracted from Tibouchina paratropica, with activities against Leishmania, anti-inflammatory, and antimicrobial properties.
Last Update: 2026-04-17 13:46:08
CAS: 1804978-82-2
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A1466937
Price: 1134, 1827, 3654 (in RMB)
Descriptions: for OX2R and OX1R, respectively. YNT-185 dihydrochloride ameliorates narcolepsy-cataplexy symptoms in mouse models[1][2].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A1466937
Price: 1134, 1827, 3654 (in RMB)
Descriptions: for OX2R and OX1R, respectively. YNT-185 dihydrochloride ameliorates narcolepsy-cataplexy symptoms in mouse models[1][2].
Last Update: 2026-04-17 13:46:08
CAS: 305820-75-1
Category: Inhibitors|Agonists, FDA-approved Compound Library
Spec: 5mg
Package: A1324931
Price: 1127 (in RMB)
Descriptions: PD173952 is a tyrosine kinase inhibitor with IC50 values of 0.3 nM, 1.7 nM, and 6.6 nM for Lyn, Abl, and Csk, respectively. It is also an inhibitor of Myt1 with a Ki of 8.1 nM and can induce apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, FDA-approved Compound Library
Spec: 5mg
Package: A1324931
Price: 1127 (in RMB)
Descriptions: PD173952 is a tyrosine kinase inhibitor with IC50 values of 0.3 nM, 1.7 nM, and 6.6 nM for Lyn, Abl, and Csk, respectively. It is also an inhibitor of Myt1 with a Ki of 8.1 nM and can induce apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 1629125-65-0
Category: Inhibitors|Agonists, Apoptosis
Spec: 2mg, 5mg, 10mg
Package: A590470
Price: 1134, 1827, 3045 (in RMB)
Descriptions: IDO-IN-4 is a potent IDO1 inhibitor with IC50 of 8 nM in human IDO1/HEK293 cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 2mg, 5mg, 10mg
Package: A590470
Price: 1134, 1827, 3045 (in RMB)
Descriptions: IDO-IN-4 is a potent IDO1 inhibitor with IC50 of 8 nM in human IDO1/HEK293 cells.
Last Update: 2026-04-17 13:46:08
CAS: 515814-01-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1167646
Price: 1139, 7576, 1071, 2835, 3686 (in RMB)
Descriptions: Voclosporin (ISAtx-247) is an inhibitor of calcineurin (CN; PP2B).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1167646
Price: 1139, 7576, 1071, 2835, 3686 (in RMB)
Descriptions: Voclosporin (ISAtx-247) is an inhibitor of calcineurin (CN; PP2B).
Last Update: 2026-04-17 13:46:08
CAS: 34408-14-5
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg
Package: A246045
Price: 1120, 1733 (in RMB)
Descriptions: 8-Chloroadenosine is a cytotoxic nucleoside analog, it can inhibit RNA synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg
Package: A246045
Price: 1120, 1733 (in RMB)
Descriptions: 8-Chloroadenosine is a cytotoxic nucleoside analog, it can inhibit RNA synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 220334-14-5
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg
Package: A1445509
Price: 1071, 1701, 3236 (in RMB)
Descriptions: Angstrom6 (A6 Peptide) is an octapeptide derived from single-chain urokinase plasminogen activator (scuPA). It interferes with the uPA/uPAR cascade and eliminates its downstream effects. Angstrom6 inhibits tumor cell migration, invasion, and metastasis by binding to CD44 and modulating CD44-mediated cell signaling.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg
Package: A1445509
Price: 1071, 1701, 3236 (in RMB)
Descriptions: Angstrom6 (A6 Peptide) is an octapeptide derived from single-chain urokinase plasminogen activator (scuPA). It interferes with the uPA/uPAR cascade and eliminates its downstream effects. Angstrom6 inhibits tumor cell migration, invasion, and metastasis by binding to CD44 and modulating CD44-mediated cell signaling.
Last Update: 2026-04-17 13:46:08
CAS: 1024828-77-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1165519
Price: 1050, 2240, 3570 (in RMB)
Descriptions: Difelikefalin (CR-845; FE-202845) is a peripherally restricted and selective agonist of kappa opioid receptor (KOR). Difelikefalin produces anti-inflammatory effects and has the potential in modulating pruritus in conditions such as chronic kidney disease.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1165519
Price: 1050, 2240, 3570 (in RMB)
Descriptions: Difelikefalin (CR-845; FE-202845) is a peripherally restricted and selective agonist of kappa opioid receptor (KOR). Difelikefalin produces anti-inflammatory effects and has the potential in modulating pruritus in conditions such as chronic kidney disease.
Last Update: 2026-04-17 13:46:08
CAS: 60314-89-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A349870
Price: 1040, 3200, 4750 (in RMB)
Descriptions: Geissoschizine methyl ether is a potent serotonin A receptor agonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A349870
Price: 1040, 3200, 4750 (in RMB)
Descriptions: Geissoschizine methyl ether is a potent serotonin A receptor agonist.
Last Update: 2026-04-17 13:46:08
CAS: 2154406-04-7
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A1537904
Price: 1031, 2268, 3717 (in RMB)
Descriptions: Zandatrigine (NBI-921352) is a sodium channel protein 8 subunit α blocker, used in neuropathological research of epilepsy and other nervous system disorders.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A1537904
Price: 1031, 2268, 3717 (in RMB)
Descriptions: Zandatrigine (NBI-921352) is a sodium channel protein 8 subunit α blocker, used in neuropathological research of epilepsy and other nervous system disorders.
Last Update: 2026-04-17 13:46:08
CAS: 23627-87-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A548147
Price: 1008, 2450, 3500 (in RMB)
Descriptions: Kaempferol-3-O-β-d-galactoside is a natural product isolated and purified from the aerial part of Calluna vulgaris L with antioxidant, anti-inflammatory and antinociceptive activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A548147
Price: 1008, 2450, 3500 (in RMB)
Descriptions: Kaempferol-3-O-β-d-galactoside is a natural product isolated and purified from the aerial part of Calluna vulgaris L with antioxidant, anti-inflammatory and antinociceptive activities.
Last Update: 2026-04-17 13:46:08
CAS: 1000999-96-1
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg
Package: A1492842
Price: 980, 2450, 3850 (in RMB)
Descriptions: Icapamespib is a heat shock protein 90 (HSP90) inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg
Package: A1492842
Price: 980, 2450, 3850 (in RMB)
Descriptions: Icapamespib is a heat shock protein 90 (HSP90) inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 33037-46-6
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg
Package: A829042
Price: 967, 2380, 3500 (in RMB)
Descriptions: Aloe-emodin-8-O-β-D-glucopyranoside is an anthraquinone compound extracted from Aloe vera with anti-inflammatory, antitumor, and antiviral activities. As an hPTP1B inhibitor, its IC50 value is 26.6 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg
Package: A829042
Price: 967, 2380, 3500 (in RMB)
Descriptions: Aloe-emodin-8-O-β-D-glucopyranoside is an anthraquinone compound extracted from Aloe vera with anti-inflammatory, antitumor, and antiviral activities. As an hPTP1B inhibitor, its IC50 value is 26.6 μM.
Last Update: 2026-04-17 13:46:08
CAS: 2955-27-3
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg
Package: A691731
Price: 960, 1440, 2970, 4132 (in RMB)
Descriptions: Ursocholic acid is a bile acid, used to study its specific activities that range from reduction of cholesterol absorpition, cholesterol gallstone dissolution to suppression of immune response.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg
Package: A691731
Price: 960, 1440, 2970, 4132 (in RMB)
Descriptions: Ursocholic acid is a bile acid, used to study its specific activities that range from reduction of cholesterol absorpition, cholesterol gallstone dissolution to suppression of immune response.
Last Update: 2026-04-17 13:46:08
CAS: 113-73-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1263653
Price: 945, 2835 (in RMB)
Descriptions: Gramicidin S is a cationic cyclic peptide antibiotic that disrupts bacterial membrane integrity, inhibits cytochrome bd quinol oxidase, and is effective against both Gram-negative and Gram-positive bacteria.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A1263653
Price: 945, 2835 (in RMB)
Descriptions: Gramicidin S is a cationic cyclic peptide antibiotic that disrupts bacterial membrane integrity, inhibits cytochrome bd quinol oxidase, and is effective against both Gram-negative and Gram-positive bacteria.
Last Update: 2026-04-17 13:46:08
CAS: 62949-77-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 2mg, 5mg, 10mg
Package: A792718
Price: 950, 1800, 2790 (in RMB)
Descriptions: Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.) and inhibits nitric oxide production with IC50 of 10.5 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 2mg, 5mg, 10mg
Package: A792718
Price: 950, 1800, 2790 (in RMB)
Descriptions: Kuwanon A is a flavone derivative isolated from the root barks of the mulberry tree (Morus alba L.) and inhibits nitric oxide production with IC50 of 10.5 μM.
Last Update: 2026-04-17 13:46:08
CAS: 25694-72-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg
Package: A282319
Price: 945, 1512, 2688 (in RMB)
Descriptions: Lonicerin is an anti-algE (alginate secretion protein) flavonoid with inhibitory activity for P. aeruginosa. Lonicerin prevents inflammation and apoptosis in LPS-induced acute lung injury.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg
Package: A282319
Price: 945, 1512, 2688 (in RMB)
Descriptions: Lonicerin is an anti-algE (alginate secretion protein) flavonoid with inhibitory activity for P. aeruginosa. Lonicerin prevents inflammation and apoptosis in LPS-induced acute lung injury.
Last Update: 2026-04-17 13:46:08
CAS: 851636-83-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1210621
Price: 945, 1480, 2835, 4397 (in RMB)
Descriptions: Cysmethynil is an indole-based Icmt time-dependent inhibitor with antitumor activity, inhibiting RAS membrane binding and EGF signaling. It induces cell cycle arrest in the G1 phase and autophagy, used for the study of solid tumors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1210621
Price: 945, 1480, 2835, 4397 (in RMB)
Descriptions: Cysmethynil is an indole-based Icmt time-dependent inhibitor with antitumor activity, inhibiting RAS membrane binding and EGF signaling. It induces cell cycle arrest in the G1 phase and autophagy, used for the study of solid tumors.
Last Update: 2026-04-17 13:46:08
CAS: 1309784-09-5
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 5mg, 10mg, 25mg, 50mg
Package: A713640
Price: 945, 1575, 3465, 5985 (in RMB)
Descriptions: ITK inhibitor 2 is a selective inhibitor of IL-2-inducible T-cell kinase (ITK, IC50 = 2 nM), which inhibits T-cell receptor signaling pathways. It may be used in research related to immune-related diseases such as autoimmune disorders or inflammation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 5mg, 10mg, 25mg, 50mg
Package: A713640
Price: 945, 1575, 3465, 5985 (in RMB)
Descriptions: ITK inhibitor 2 is a selective inhibitor of IL-2-inducible T-cell kinase (ITK, IC50 = 2 nM), which inhibits T-cell receptor signaling pathways. It may be used in research related to immune-related diseases such as autoimmune disorders or inflammation.
Last Update: 2026-04-17 13:46:08
CAS: 76252-06-7
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg
Package: A385536
Price: 931, 2359 (in RMB)
Descriptions: Nicainoprol is a sodium channels blocker which is used as an antiarrhythmic agent.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg
Package: A385536
Price: 931, 2359 (in RMB)
Descriptions: Nicainoprol is a sodium channels blocker which is used as an antiarrhythmic agent.
Last Update: 2026-04-17 13:46:08
CAS: 409086-68-6
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg, 25mg
Package: A1399071
Price: 945, 1575, 3465 (in RMB)
Descriptions: YM-1 is an analog of MKT-077 with oral bioactivity that can stabilize Hsp70 inhibition. YM-1 induces cell death in HeLa cells while upregulating p53 and p21 protein levels, making it suitable for cancer research related to Hsp70.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg, 25mg
Package: A1399071
Price: 945, 1575, 3465 (in RMB)
Descriptions: YM-1 is an analog of MKT-077 with oral bioactivity that can stabilize Hsp70 inhibition. YM-1 induces cell death in HeLa cells while upregulating p53 and p21 protein levels, making it suitable for cancer research related to Hsp70.
Last Update: 2026-04-17 13:46:08
CAS: 1016340-64-9
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1124391
Price: 917, 1379, 2751, 4130 (in RMB)
Descriptions: Z57346765 is a highly specific inhibitor of phosphoglycerate kinase 1 (PGK1). By targeting PGK1, it cuts off the "energy supply line" that cancer cells rely on for rapid growth. It inhibits the activity of a key enzyme in glycolysis, reduces ATP production, induces metabolic stress, and thereby suppresses the proliferation and survival of cancer cells, including in clear cell renal cell carcinoma.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1124391
Price: 917, 1379, 2751, 4130 (in RMB)
Descriptions: Z57346765 is a highly specific inhibitor of phosphoglycerate kinase 1 (PGK1). By targeting PGK1, it cuts off the "energy supply line" that cancer cells rely on for rapid growth. It inhibits the activity of a key enzyme in glycolysis, reduces ATP production, induces metabolic stress, and thereby suppresses the proliferation and survival of cancer cells, including in clear cell renal cell carcinoma.
Last Update: 2026-04-17 13:46:08
CAS: 869490-23-3
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg
Package: A1371186
Price: 896 (in RMB)
Descriptions: Metabolic Disease
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg
Package: A1371186
Price: 896 (in RMB)
Descriptions: Metabolic Disease
Last Update: 2026-04-17 13:46:08
CAS: 952565-91-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1176683
Price: 907, 1960, 2940 (in RMB)
Descriptions: ASP-4058 is a selective, orally active S1P1 and S1P5 agonist that significantly improves experimental autoimmune encephalomyelitis models, demonstrating good safety and applicability in autoimmune disease research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1176683
Price: 907, 1960, 2940 (in RMB)
Descriptions: ASP-4058 is a selective, orally active S1P1 and S1P5 agonist that significantly improves experimental autoimmune encephalomyelitis models, demonstrating good safety and applicability in autoimmune disease research.
Last Update: 2026-04-17 13:46:08
CAS: 6681-13-6
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg
Package: A1144488
Price: 874, 2181 (in RMB)
Descriptions: Hernandezine is an alkaloid derived from Tripterygium species with anti-inflammatory, antioxidant, and anticancer activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg
Package: A1144488
Price: 874, 2181 (in RMB)
Descriptions: Hernandezine is an alkaloid derived from Tripterygium species with anti-inflammatory, antioxidant, and anticancer activities.
Last Update: 2026-04-17 13:46:08
CAS: 105650-23-5
Category: Natural product, By Structure
Spec: 1mg, 5mg, 10mg
Package: A116374
Price: 854, 1750, 2450 (in RMB)
Descriptions: PhIP is a heterocyclic aromatic amine (HAA) derived from cooked meat, belonging to the pyridine class of heterocyclic amines. It is a class 2B carcinogen with estrogenic activity and can form DNA adducts, promoting cancer development.
Last Update: 2026-04-17 13:46:08
Category: Natural product, By Structure
Spec: 1mg, 5mg, 10mg
Package: A116374
Price: 854, 1750, 2450 (in RMB)
Descriptions: PhIP is a heterocyclic aromatic amine (HAA) derived from cooked meat, belonging to the pyridine class of heterocyclic amines. It is a class 2B carcinogen with estrogenic activity and can form DNA adducts, promoting cancer development.
Last Update: 2026-04-17 13:46:08
CAS: 1332391-11-3
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg
Package: A1364782
Price: 872, 1952, 2967 (in RMB)
Descriptions: N-Desmethyl Apalutamide is the active metabolite of Apalutamide, with an efficacy approximately one-third that of the parent drug. It is formed through the action of CYP2C8 and CYP3A4, exhibiting moderate to strong induction effects on CYP3A4 and CYP2B6, along with high plasma protein binding capability, making it suitable for studies on the metabolism and drug interactions of androgen receptor inhibitors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg
Package: A1364782
Price: 872, 1952, 2967 (in RMB)
Descriptions: N-Desmethyl Apalutamide is the active metabolite of Apalutamide, with an efficacy approximately one-third that of the parent drug. It is formed through the action of CYP2C8 and CYP3A4, exhibiting moderate to strong induction effects on CYP3A4 and CYP2B6, along with high plasma protein binding capability, making it suitable for studies on the metabolism and drug interactions of androgen receptor inhibitors.
Last Update: 2026-04-17 13:46:08
CAS: 2226941-26-8
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A2021568
Price: 850, 2016, 3213 (in RMB)
Descriptions: THK01 is an efficient ROCK2 inhibitor with IC50 values of 5.7 nM (ROCK2) and 923 nM (ROCK1). It inhibits breast cancer metastasis through the ROCK2-STAT3 signaling pathway and is widely used in breast cancer research, especially in studies exploring tumor metastasis mechanisms.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A2021568
Price: 850, 2016, 3213 (in RMB)
Descriptions: THK01 is an efficient ROCK2 inhibitor with IC50 values of 5.7 nM (ROCK2) and 923 nM (ROCK1). It inhibits breast cancer metastasis through the ROCK2-STAT3 signaling pathway and is widely used in breast cancer research, especially in studies exploring tumor metastasis mechanisms.
Last Update: 2026-04-17 13:46:08
CAS: 2201057-10-3
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A711197
Price: 840, 2030, 3220 (in RMB)
Descriptions: MAT2A inhibitor is a methionine adenosyltransferase 2A (MATA2) inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A711197
Price: 840, 2030, 3220 (in RMB)
Descriptions: MAT2A inhibitor is a methionine adenosyltransferase 2A (MATA2) inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 6743-92-6
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A298580
Price: 840, 2240, 3640 (in RMB)
Descriptions: Isorhamnetin-3-O-galactoside and persicarin have an effect on down-regulation of endothelial protein C receptor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A298580
Price: 840, 2240, 3640 (in RMB)
Descriptions: Isorhamnetin-3-O-galactoside and persicarin have an effect on down-regulation of endothelial protein C receptor.
Last Update: 2026-04-17 13:46:08
CAS: 1366302-52-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1481280
Price: 844, 1772, 2835, 5387 (in RMB)
Descriptions: PSMA-11 is a ligand to make gallium Ga 68-labeled PSMA-11, which has potential use as a tracer for PSMA-expressing tumors during positron emission tomography.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1481280
Price: 844, 1772, 2835, 5387 (in RMB)
Descriptions: PSMA-11 is a ligand to make gallium Ga 68-labeled PSMA-11, which has potential use as a tracer for PSMA-expressing tumors during positron emission tomography.
Last Update: 2026-04-17 13:46:08
CAS: 315703-81-2
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A1227206
Price: 760, 1760 (in RMB)
Descriptions: WAY-118959-A is a tubulin acetylation inhibitor that directly binds α-tubulin and prevents α-tubulin acetyltransferase 1 (αTAT1) from acting on the K40 residue of α-tubulin. GM-90257 induces apoptosis in MDA-MB-231 cells while having minimal effects on MCF-10A or MCF-7 cells with lower levels of tubulin acetylation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg
Package: A1227206
Price: 760, 1760 (in RMB)
Descriptions: WAY-118959-A is a tubulin acetylation inhibitor that directly binds α-tubulin and prevents α-tubulin acetyltransferase 1 (αTAT1) from acting on the K40 residue of α-tubulin. GM-90257 induces apoptosis in MDA-MB-231 cells while having minimal effects on MCF-10A or MCF-7 cells with lower levels of tubulin acetylation.
Last Update: 2026-04-17 13:46:08
CAS: 356102-14-2
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1263761
Price: 787, 1260, 2646, 4221 (in RMB)
Descriptions: Ani 9 is selective TMEM16A blocker with IC50 of 77 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1263761
Price: 787, 1260, 2646, 4221 (in RMB)
Descriptions: Ani 9 is selective TMEM16A blocker with IC50 of 77 nM.
Last Update: 2026-04-17 13:46:08
CAS: 2345-17-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A806823
Price: 819, 1858, 2822 (in RMB)
Descriptions: Irisolidone is isolated from the flower of pueraria lobata (Kudzu) with anti-inflammatory activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A806823
Price: 819, 1858, 2822 (in RMB)
Descriptions: Irisolidone is isolated from the flower of pueraria lobata (Kudzu) with anti-inflammatory activity.
Last Update: 2026-04-17 13:46:08
CAS: 863971-12-4
Category: Inhibitors|Agonists, Antibody-drug Conjugate|ADC Related
Spec: 10mg, 25mg, 50mg, 100mg, 250mg
Package: A700623
Price: 830, 1659, 2820, 4794, 9107 (in RMB)
Descriptions: MMAF-OMe is a synthetic antineoplastic agent and also used as a part of some experimental anti-cancer antibody-drug conjugates such as vorsetuzumab mafodotin and SGN-CD19A.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Antibody-drug Conjugate|ADC Related
Spec: 10mg, 25mg, 50mg, 100mg, 250mg
Package: A700623
Price: 830, 1659, 2820, 4794, 9107 (in RMB)
Descriptions: MMAF-OMe is a synthetic antineoplastic agent and also used as a part of some experimental anti-cancer antibody-drug conjugates such as vorsetuzumab mafodotin and SGN-CD19A.
Last Update: 2026-04-17 13:46:08
CAS: 30358-88-4
Category: Natural product, Hernandiaceae
Spec: 1mg, 5mg, 10mg
Package: A1144399
Price: 758, 1991, 3389 (in RMB)
Descriptions: 3'-O-Acetylhamaudol is a natural compound extracted from Angelica polymorpha, with antitumor activity.
Last Update: 2026-04-17 13:46:08
Category: Natural product, Hernandiaceae
Spec: 1mg, 5mg, 10mg
Package: A1144399
Price: 758, 1991, 3389 (in RMB)
Descriptions: 3'-O-Acetylhamaudol is a natural compound extracted from Angelica polymorpha, with antitumor activity.
Last Update: 2026-04-17 13:46:08
CAS: 29307-03-7
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg
Package: A838524
Price: 756, 1890, 2929 (in RMB)
Descriptions: Deoxyelephantopin is a natural product isolated and purified from the herbs of Elephantopus scaber Linn. with hepatoprotective and antitumor activity, by inhibiting metastatic, inducing apoptosis, modulating oxidative stress , STAT3/p53/p21 signaling, MAPK pathway, PI3k/Akt/mTOR pathway, caspase cascades, and ROS .
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg
Package: A838524
Price: 756, 1890, 2929 (in RMB)
Descriptions: Deoxyelephantopin is a natural product isolated and purified from the herbs of Elephantopus scaber Linn. with hepatoprotective and antitumor activity, by inhibiting metastatic, inducing apoptosis, modulating oxidative stress , STAT3/p53/p21 signaling, MAPK pathway, PI3k/Akt/mTOR pathway, caspase cascades, and ROS .
Last Update: 2026-04-17 13:46:08
CAS: 69120-06-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A784508
Price: 742, 2246 (in RMB)
Descriptions: Moracin C, a natural product isolated and purified from the root bark of Morus alba L., is a potent antibacterial compound which inhibits FabI and fatty acid synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A784508
Price: 742, 2246 (in RMB)
Descriptions: Moracin C, a natural product isolated and purified from the root bark of Morus alba L., is a potent antibacterial compound which inhibits FabI and fatty acid synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 2359649-81-1
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg, 10mg
Package: A1603075
Price: 732, 1780, 2630 (in RMB)
Descriptions: Enbezotinib is a targeted tyrosine kinase inhibitor (TKI) targeting BCR-ABL, FLT3, etc., used in chronic myeloid leukemia (CML) or other related hematological malignancies.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg, 10mg
Package: A1603075
Price: 732, 1780, 2630 (in RMB)
Descriptions: Enbezotinib is a targeted tyrosine kinase inhibitor (TKI) targeting BCR-ABL, FLT3, etc., used in chronic myeloid leukemia (CML) or other related hematological malignancies.
Last Update: 2026-04-17 13:46:08
CAS: 2361139-70-8
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1339731
Price: 735, 1470, 2450, 4690 (in RMB)
Descriptions: RIPK3-IN-1 is a RIPK3 type II DFG-out inhibitor with an IC50 of 9.1 nM. RIPK3-IN-1 inhibits RIPK1 and RIPK2 with IC50s of 5.5 and >10 μM. RIPK3-IN-1 is also a c-Met kinase inhibitor with an IC50 of 1.1 μM[1].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1339731
Price: 735, 1470, 2450, 4690 (in RMB)
Descriptions: RIPK3-IN-1 is a RIPK3 type II DFG-out inhibitor with an IC50 of 9.1 nM. RIPK3-IN-1 inhibits RIPK1 and RIPK2 with IC50s of 5.5 and >10 μM. RIPK3-IN-1 is also a c-Met kinase inhibitor with an IC50 of 1.1 μM[1].
Last Update: 2026-04-17 13:46:08
CAS: 2004-04-8
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A376932
Price: 720, 2040, 3456 (in RMB)
Descriptions: Angustmycin A is a nucleoside-analog inhibitor of GMPS (guanosine monophosphate synthase) produced by Streptomyces hygroscopius that efficiently suppresses melanoma cell invasion in vitro and tumorigenicity in immunocompromised mice.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A376932
Price: 720, 2040, 3456 (in RMB)
Descriptions: Angustmycin A is a nucleoside-analog inhibitor of GMPS (guanosine monophosphate synthase) produced by Streptomyces hygroscopius that efficiently suppresses melanoma cell invasion in vitro and tumorigenicity in immunocompromised mice.
Last Update: 2026-04-17 13:46:08
CAS: 171485-39-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A153206
Price: 709, 1134, 1927, 3276 (in RMB)
Descriptions: Myrislignan is a natural product with antifungal properties, it's isolated and purified from the seeds of Myristica fragrans Houtt..
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A153206
Price: 709, 1134, 1927, 3276 (in RMB)
Descriptions: Myrislignan is a natural product with antifungal properties, it's isolated and purified from the seeds of Myristica fragrans Houtt..
Last Update: 2026-04-17 13:46:08
CAS: 14965-20-9
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A696070
Price: 700, 1750, 2730 (in RMB)
Descriptions: Chrysosplenol D is a methoxyflavone compound that induces ERK1/2-mediated apoptosis in triple-negative human breast cancer cells. It also exhibits anti-inflammatory and moderate antitrypanosomal activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 5mg, 10mg
Package: A696070
Price: 700, 1750, 2730 (in RMB)
Descriptions: Chrysosplenol D is a methoxyflavone compound that induces ERK1/2-mediated apoptosis in triple-negative human breast cancer cells. It also exhibits anti-inflammatory and moderate antitrypanosomal activities.
Last Update: 2026-04-17 13:46:08
CAS: 2803211-60-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1602537
Price: 700, 1050, 2100, 3360 (in RMB)
Descriptions: GRP-60367 hydrochloride is a first-in-class small molecule inhibitor of rabies virus (RABV) entry, specifically targeting the RABV G protein. It is applicable for research on rabies virus.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1602537
Price: 700, 1050, 2100, 3360 (in RMB)
Descriptions: GRP-60367 hydrochloride is a first-in-class small molecule inhibitor of rabies virus (RABV) entry, specifically targeting the RABV G protein. It is applicable for research on rabies virus.
Last Update: 2026-04-17 13:46:08
CAS: 559-74-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A428182
Price: 700, 1400, 2240, 3584 (in RMB)
Descriptions: Friedelin, a natural product isolated and purified from the herbs of Celastrus stylosus Wall., possesses potent anti-inflammatory, analgesic and antipyretic activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A428182
Price: 700, 1400, 2240, 3584 (in RMB)
Descriptions: Friedelin, a natural product isolated and purified from the herbs of Celastrus stylosus Wall., possesses potent anti-inflammatory, analgesic and antipyretic activities.
Last Update: 2026-04-17 13:46:08
CAS: 1809427-20-0
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg
Package: A1176955
Price: 700, 1960, 2744 (in RMB)
Descriptions: (1S,2S,3R)-DT-061 is an enantiomer of DT-061, an orally active activator of protein phosphatase 2A (PP2A). It can be used as a negative control to study KRAS mutations and MYC-driven lung cancer tumors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg
Package: A1176955
Price: 700, 1960, 2744 (in RMB)
Descriptions: (1S,2S,3R)-DT-061 is an enantiomer of DT-061, an orally active activator of protein phosphatase 2A (PP2A). It can be used as a negative control to study KRAS mutations and MYC-driven lung cancer tumors.
Last Update: 2026-04-17 13:46:08
CAS: 68236-13-5
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg
Package: A1144461
Price: 698, 1859, 2790 (in RMB)
Descriptions: (2S)-6-Prenylnaringenin is the most potent compound in the forebrain, acting as a GABAA receptor PAM at the α+β binding site.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg
Package: A1144461
Price: 698, 1859, 2790 (in RMB)
Descriptions: (2S)-6-Prenylnaringenin is the most potent compound in the forebrain, acting as a GABAA receptor PAM at the α+β binding site.
Last Update: 2026-04-17 13:46:08
CAS: 887148-69-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A949820
Price: 686, 2170, 3185 (in RMB)
Descriptions: Monepantel is organic anthelmintic, and acts as a positive allosteric modulator of a nematode-specific clade of nicotinic acetylcholine receptor (nAChR) subunits.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A949820
Price: 686, 2170, 3185 (in RMB)
Descriptions: Monepantel is organic anthelmintic, and acts as a positive allosteric modulator of a nematode-specific clade of nicotinic acetylcholine receptor (nAChR) subunits.
Last Update: 2026-04-17 13:46:08
CAS: 94356-22-6
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg
Package: A987492
Price: 665, 1680 (in RMB)
Descriptions: Rhapontigenin 3'-O-glucoside is a derivative of Rhapontigenin, which is a potent P450 1A1 inhibitor and may be useful in cancer prevention.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg
Package: A987492
Price: 665, 1680 (in RMB)
Descriptions: Rhapontigenin 3'-O-glucoside is a derivative of Rhapontigenin, which is a potent P450 1A1 inhibitor and may be useful in cancer prevention.
Last Update: 2026-04-17 13:46:08
CAS: 41552-95-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A458692
Price: 678, 1514, 2179 (in RMB)
Descriptions: A2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A458692
Price: 678, 1514, 2179 (in RMB)
Descriptions: A2AR-agonist-1 is a potent A2AR and ENT1 agonist with Ki of 4.39 and 3.47 for A2AR and ENT1.
Last Update: 2026-04-17 13:46:08
CAS: 191034-25-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A580638
Price: 644, 1417, 2205, 4183 (in RMB)
Descriptions: L-168,049 is a very potent and selective, non-competitive antagonist of the human glucagon receptor with IC50 of 3.7 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A580638
Price: 644, 1417, 2205, 4183 (in RMB)
Descriptions: L-168,049 is a very potent and selective, non-competitive antagonist of the human glucagon receptor with IC50 of 3.7 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1417162-36-7
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg
Package: A714632
Price: 658, 1645, 2800 (in RMB)
Descriptions: RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA binding assay and specifically inhibits HR (Homologous recombination) repair in human cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 1mg, 5mg, 10mg
Package: A714632
Price: 658, 1645, 2800 (in RMB)
Descriptions: RI-2 is an optimized RAD51 inhibitor with an IC50 of 44.17 μM in the standard DNA binding assay and specifically inhibits HR (Homologous recombination) repair in human cells.
Last Update: 2026-04-17 13:46:08
CAS: 894783-71-2
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A965239
Price: 642, 942, 1780, 2690, 3830 (in RMB)
Descriptions: BIBF 1202 is the carboxylate metabolite of BIBF 1120, which is an oral triple angiokinase inhibitor targeting VEGFR, PDGFR, FGFR.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A965239
Price: 642, 942, 1780, 2690, 3830 (in RMB)
Descriptions: BIBF 1202 is the carboxylate metabolite of BIBF 1120, which is an oral triple angiokinase inhibitor targeting VEGFR, PDGFR, FGFR.
Last Update: 2026-04-17 13:46:08
CAS: 2064269-82-3
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg
Package: A2420741
Price: 639, 4240, 1386, 3465 (in RMB)
Descriptions: YK-029A is an orally effective EGFR mutation inhibitor targeting T790M mutations and exon 20 insertions, demonstrating significant antitumor activity in driven PDX models.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg
Package: A2420741
Price: 639, 4240, 1386, 3465 (in RMB)
Descriptions: YK-029A is an orally effective EGFR mutation inhibitor targeting T790M mutations and exon 20 insertions, demonstrating significant antitumor activity in driven PDX models.
Last Update: 2026-04-17 13:46:08
CAS: 355151-12-1
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 50μL, 1mL, 1mg, 5mg
Package: A1365216
Price: 639, 4277, 945, 2835 (in RMB)
Descriptions: Rotigaptide is a specific connexin 43 (Cx43) modulator that prevents Cx43-mediated gap junction communication uncoupling and restores normal intercellular communication during acute metabolic stress. This peptide compound has potential applications in arrhythmias, particularly atrial fibrillation research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cytoskeleton Signaling Pathway
Spec: 50μL, 1mL, 1mg, 5mg
Package: A1365216
Price: 639, 4277, 945, 2835 (in RMB)
Descriptions: Rotigaptide is a specific connexin 43 (Cx43) modulator that prevents Cx43-mediated gap junction communication uncoupling and restores normal intercellular communication during acute metabolic stress. This peptide compound has potential applications in arrhythmias, particularly atrial fibrillation research.
Last Update: 2026-04-17 13:46:08
CAS: 37693-01-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 500mg
Package: A399190
Price: 630, 1960 (in RMB)
Descriptions: Clofoctol is a bacteriostatic antibiotic. It is used in the treatment of respiratory tract and ear, nose and throat infections caused by Gram-positive bacteria. It is only functional against Gram-positive bacteria, It penetrates into human lung tissue.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 500mg
Package: A399190
Price: 630, 1960 (in RMB)
Descriptions: Clofoctol is a bacteriostatic antibiotic. It is used in the treatment of respiratory tract and ear, nose and throat infections caused by Gram-positive bacteria. It is only functional against Gram-positive bacteria, It penetrates into human lung tissue.
Last Update: 2026-04-17 13:46:08
CAS: 2685795-52-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1602866
Price: 630, 1008, 2150, 3180, 4680 (in RMB)
Descriptions: SDH-IN-1 is a succinate dehydrogenase (SDH) inhibitor with an IC50 of 4.53 μM, exhibiting antifungal activity, particularly effective against S. sclerotiorum (EC50 = 0.14 mg/L), suitable for antifungal treatment research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1602866
Price: 630, 1008, 2150, 3180, 4680 (in RMB)
Descriptions: SDH-IN-1 is a succinate dehydrogenase (SDH) inhibitor with an IC50 of 4.53 μM, exhibiting antifungal activity, particularly effective against S. sclerotiorum (EC50 = 0.14 mg/L), suitable for antifungal treatment research.
Last Update: 2026-04-17 13:46:08
CAS: 70763-62-1
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1210299
Price: 630, 1386, 2268, 4536 (in RMB)
Descriptions: 2-deoxy-2-fluoro L-Fucose is a fluorinated fucose analog which can be metabolized inside the cell to a substrate-based inhibitor of fucosyltransferases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1210299
Price: 630, 1386, 2268, 4536 (in RMB)
Descriptions: 2-deoxy-2-fluoro L-Fucose is a fluorinated fucose analog which can be metabolized inside the cell to a substrate-based inhibitor of fucosyltransferases.
Last Update: 2026-04-17 13:46:08
CAS: 871266-63-6
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A889136
Price: 630, 1134, 1890, 3076, 4366, 6112 (in RMB)
Descriptions: PCI-27483 is a FVIIa/tissue factor inhibitor with antitumour effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A889136
Price: 630, 1134, 1890, 3076, 4366, 6112 (in RMB)
Descriptions: PCI-27483 is a FVIIa/tissue factor inhibitor with antitumour effects.
Last Update: 2026-04-17 13:46:08
CAS: 34532-68-8
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg
Package: A737788
Price: 630, 1890, 3024 (in RMB)
Descriptions: Arnicolide D is a sesquiterpene lactone extracted from Arnica montana, capable of regulating the cell cycle, activating the caspase signaling pathway, and inhibiting the PI3K/AKT and STAT3 pathways, demonstrating inhibitory effects on nasopharyngeal carcinoma cell growth.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg
Package: A737788
Price: 630, 1890, 3024 (in RMB)
Descriptions: Arnicolide D is a sesquiterpene lactone extracted from Arnica montana, capable of regulating the cell cycle, activating the caspase signaling pathway, and inhibiting the PI3K/AKT and STAT3 pathways, demonstrating inhibitory effects on nasopharyngeal carcinoma cell growth.
Last Update: 2026-04-17 13:46:08
CAS: 1354691-97-6
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1892731
Price: 624, 1134, 1827, 3837 (in RMB)
Descriptions: Leniolisib phosphate is a potent and selective PI3Kδ inhibitor, with potential applications in immunodeficiency disease research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1892731
Price: 624, 1134, 1827, 3837 (in RMB)
Descriptions: Leniolisib phosphate is a potent and selective PI3Kδ inhibitor, with potential applications in immunodeficiency disease research.
Last Update: 2026-04-17 13:46:08
CAS: 60084-10-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg
Package: A479093
Price: 630, 1050 (in RMB)
Descriptions: Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg
Package: A479093
Price: 630, 1050 (in RMB)
Descriptions: Tiazofurin is a synthetic nucleoside analogue with antineoplastic activity.
Last Update: 2026-04-17 13:46:08
CAS: 109437-62-9
Category: Inhibitors|Agonists, Apoptosis
Spec: 10mg, 25mg, 50mg, 100mg
Package: A207293
Price: 595, 892, 1339, 2009 (in RMB)
Descriptions: ALDH1A inhibitor 673A is a potent ALDH1A inhibitor, exhibiting significant inhibition of ALDH1A1, ALDH1A2, and ALDH1A3, inducing cancer stem cell necrosis and inhibiting the growth of chemotherapy-resistant tumors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 10mg, 25mg, 50mg, 100mg
Package: A207293
Price: 595, 892, 1339, 2009 (in RMB)
Descriptions: ALDH1A inhibitor 673A is a potent ALDH1A inhibitor, exhibiting significant inhibition of ALDH1A1, ALDH1A2, and ALDH1A3, inducing cancer stem cell necrosis and inhibiting the growth of chemotherapy-resistant tumors.
Last Update: 2026-04-17 13:46:08
CAS: 676500-67-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A119986
Price: 592, 1380, 1980 (in RMB)
Descriptions: Bevenopran is a peripheral μ-opioid receptor antagonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A119986
Price: 592, 1380, 1980 (in RMB)
Descriptions: Bevenopran is a peripheral μ-opioid receptor antagonist.
Last Update: 2026-04-17 13:46:08
CAS: 923417-09-8
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg, 50mg
Package: A2410065
Price: 592, 990, 1970, 2830 (in RMB)
Descriptions: VU533 is a potent NAPE-PLD activator with an EC50 of 0.30 µM, enhancing macrophage phagocytosis, suitable for research on cardiac metabolic diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 5mg, 10mg, 25mg, 50mg
Package: A2410065
Price: 592, 990, 1970, 2830 (in RMB)
Descriptions: VU533 is a potent NAPE-PLD activator with an EC50 of 0.30 µM, enhancing macrophage phagocytosis, suitable for research on cardiac metabolic diseases.
Last Update: 2026-04-17 13:46:08
CAS: 134296-40-5
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg
Package: A877668
Price: 573 (in RMB)
Descriptions: BIMU 8 is a potent 5-HT4 receptor full agonist with KD of 77 nM and EC50 of 18 nM for wild type 5-HT4 receptors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg
Package: A877668
Price: 573 (in RMB)
Descriptions: BIMU 8 is a potent 5-HT4 receptor full agonist with KD of 77 nM and EC50 of 18 nM for wild type 5-HT4 receptors.
Last Update: 2026-04-17 13:46:08
CAS: 31362-50-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A421644
Price: 567, 1134, 1764, 2800 (in RMB)
Descriptions: Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A421644
Price: 567, 1134, 1764, 2800 (in RMB)
Descriptions: Bombesin, a tetradecapeptide originally isolated from frog skin, has an important role in the release of gastrin and the activation of G-protein receptors.
Last Update: 2026-04-17 13:46:08
CAS: 92077-78-6
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 1mg, 5mg
Package: A101641
Price: 570, 1596 (in RMB)
Descriptions: Cilazapril is an angiotensin-converting enzyme (ACE) inhibitor used for the treatment of hypertension and congestive heart failure.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Endocrinology|Hormones
Spec: 1mg, 5mg
Package: A101641
Price: 570, 1596 (in RMB)
Descriptions: Cilazapril is an angiotensin-converting enzyme (ACE) inhibitor used for the treatment of hypertension and congestive heart failure.
Last Update: 2026-04-17 13:46:08
CAS: 1334526-14-5
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A951251
Price: 559, 1320, 1715, 2798, 4067, 6101 (in RMB)
Descriptions: (±)-ML 209 is a RORγt inverse agonist with IC50 of 460 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A951251
Price: 559, 1320, 1715, 2798, 4067, 6101 (in RMB)
Descriptions: (±)-ML 209 is a RORγt inverse agonist with IC50 of 460 nM.
Last Update: 2026-04-17 13:46:08
CAS: 101622-51-9
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A912269
Price: 525, 1260, 2016 (in RMB)
Descriptions: Olomoucine is an ATP-competitive CDK inhibitor that inhibits the activity of CDC2/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, and ERK1/p44 MAPK, regulating the cell cycle and showing potential in melanoma treatment.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A912269
Price: 525, 1260, 2016 (in RMB)
Descriptions: Olomoucine is an ATP-competitive CDK inhibitor that inhibits the activity of CDC2/cyclin B, Cdk2/cyclin A, Cdk2/cyclin E, and ERK1/p44 MAPK, regulating the cell cycle and showing potential in melanoma treatment.
Last Update: 2026-04-17 13:46:08
CAS: 592-95-0
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg
Package: A470006
Price: 504, 756, 1386 (in RMB)
Descriptions: Sulforaphene is a natural isothiocyanate found in cruciferous vegetables.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg
Package: A470006
Price: 504, 756, 1386 (in RMB)
Descriptions: Sulforaphene is a natural isothiocyanate found in cruciferous vegetables.
Last Update: 2026-04-17 13:46:08
CAS: 29679-58-1
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 100mg
Package: A244887
Price: 501 (in RMB)
Descriptions: Fenoprofen (LILLY-53858) is a non-steroidal anti-inflammatory drug (NSAID) used to relieve symptoms of osteoarthritis and rheumatoid arthritis, including inflammation, swelling, stiffness, and joint pain. Fenoprofen also acts as an allosteric enhancer of melanocortin receptors and promotes ERK1/2 activation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 100mg
Package: A244887
Price: 501 (in RMB)
Descriptions: Fenoprofen (LILLY-53858) is a non-steroidal anti-inflammatory drug (NSAID) used to relieve symptoms of osteoarthritis and rheumatoid arthritis, including inflammation, swelling, stiffness, and joint pain. Fenoprofen also acts as an allosteric enhancer of melanocortin receptors and promotes ERK1/2 activation.
Last Update: 2026-04-17 13:46:08
CAS: 18842-98-3
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 5mg, 10mg, 25mg
Package: A755503
Price: 500, 800, 1575 (in RMB)
Descriptions: Paederosidic acid has anti-tumor, anticonvulsant and sedative effects. It may be a promising future therapeutic agent for treatment of epilepsy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 5mg, 10mg, 25mg
Package: A755503
Price: 500, 800, 1575 (in RMB)
Descriptions: Paederosidic acid has anti-tumor, anticonvulsant and sedative effects. It may be a promising future therapeutic agent for treatment of epilepsy.
Last Update: 2026-04-17 13:46:08
CAS: 2409964-23-2
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1549546
Price: 497, 945, 1575, 2835 (in RMB)
Descriptions: LOX-IN-3 dihydrochloride is an orally active inhibitor of lysyl oxidase (LOX), used in research on fibrosis, cancer, and angiogenesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 1mg, 5mg, 10mg, 25mg
Package: A1549546
Price: 497, 945, 1575, 2835 (in RMB)
Descriptions: LOX-IN-3 dihydrochloride is an orally active inhibitor of lysyl oxidase (LOX), used in research on fibrosis, cancer, and angiogenesis.
Last Update: 2026-04-17 13:46:08
CAS: 26091-79-2
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg
Package: A782383
Price: 499, 1225, 1960, 3000 (in RMB)
Descriptions: Byakangelicol is isolated from the roots of Angelica dahurica with hepatoprotective activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg
Package: A782383
Price: 499, 1225, 1960, 3000 (in RMB)
Descriptions: Byakangelicol is isolated from the roots of Angelica dahurica with hepatoprotective activities.
Last Update: 2026-04-17 13:46:08
CAS: 5875-49-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A141657
Price: 490, 1260 (in RMB)
Descriptions: Meranzin, a natural product isolated and purified from the roots of Angelica biserrata, produces a rapid effect mediated by AMPA receptors and involving BDNF modulation through the ERK1/2 pathway. Meranzin can also induce similar effect to Fructus Aurantii on intestinal motility and it was, at least in part, mediated by stimulation of H1 histamine receptors, and exhibits antidepressive and prokinetic-like effects through the regulation of the common mediator, the alpha 2-adrenoceptor , and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg
Package: A141657
Price: 490, 1260 (in RMB)
Descriptions: Meranzin, a natural product isolated and purified from the roots of Angelica biserrata, produces a rapid effect mediated by AMPA receptors and involving BDNF modulation through the ERK1/2 pathway. Meranzin can also induce similar effect to Fructus Aurantii on intestinal motility and it was, at least in part, mediated by stimulation of H1 histamine receptors, and exhibits antidepressive and prokinetic-like effects through the regulation of the common mediator, the alpha 2-adrenoceptor , and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors.
Last Update: 2026-04-17 13:46:08
CAS: 18719-76-1
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg
Package: A857431
Price: 489, 1365 (in RMB)
Descriptions: Keracyanin chloride (Cyanidin 3-rutinoside chloride) is an anthocyanin with antioxidant properties. It can inhibit the formation of malondialdehyde in oxidized calf thymus DNA.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg
Package: A857431
Price: 489, 1365 (in RMB)
Descriptions: Keracyanin chloride (Cyanidin 3-rutinoside chloride) is an anthocyanin with antioxidant properties. It can inhibit the formation of malondialdehyde in oxidized calf thymus DNA.
Last Update: 2026-04-17 13:46:08
CAS: 612542-14-0
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1155088
Price: 489, 3240, 1085, 2800, 4730 (in RMB)
Descriptions: Hh-Ag1.5 is a highly efficient Hedgehog (Hh) agonist with an EC50 of 1 nM, capable of breaking the quiescent state of non-injured liver stem cells through mediation of reprogramming, thus rescuing liver failure.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1155088
Price: 489, 3240, 1085, 2800, 4730 (in RMB)
Descriptions: Hh-Ag1.5 is a highly efficient Hedgehog (Hh) agonist with an EC50 of 1 nM, capable of breaking the quiescent state of non-injured liver stem cells through mediation of reprogramming, thus rescuing liver failure.
Last Update: 2026-04-17 13:46:08
CAS: 36707-00-3
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg
Package: A991434
Price: 485 (in RMB)
Descriptions: API-1 is a selective Akt/PKB inhibitor and shows antitumor activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg
Package: A991434
Price: 485 (in RMB)
Descriptions: API-1 is a selective Akt/PKB inhibitor and shows antitumor activity.
Last Update: 2026-04-17 13:46:08
CAS: 89919-62-0
Category: Natural product, Asteraceae
Spec: 1mg, 5mg, 10mg
Package: A768804
Price: 479, 1260, 1864 (in RMB)
Descriptions: 3,5-O-Dicaffeoylquinic acid (Isochlorogenic Acid A) reverses learning and memory deficits induced by Trimethyltin.
Last Update: 2026-04-17 13:46:08
Category: Natural product, Asteraceae
Spec: 1mg, 5mg, 10mg
Package: A768804
Price: 479, 1260, 1864 (in RMB)
Descriptions: 3,5-O-Dicaffeoylquinic acid (Isochlorogenic Acid A) reverses learning and memory deficits induced by Trimethyltin.
Last Update: 2026-04-17 13:46:08
CAS: 38840-23-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A985678
Price: 480, 1164, 1864 (in RMB)
Descriptions: Emodin-1-O-β-D-glucopyranoside, extracted from the medicinal plant Polygonum cuspidatum, is an effective and non-competitive bacterial neuraminidase (BNA) inhibitor with an IC50 value of 0.85 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A985678
Price: 480, 1164, 1864 (in RMB)
Descriptions: Emodin-1-O-β-D-glucopyranoside, extracted from the medicinal plant Polygonum cuspidatum, is an effective and non-competitive bacterial neuraminidase (BNA) inhibitor with an IC50 value of 0.85 μM.
Last Update: 2026-04-17 13:46:08
CAS: 2711006-67-4
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg, 5mg, 10mg
Package: A1601835
Price: 475, 1330, 2170 (in RMB)
Descriptions: ZXH-4-130 TFA is a highly potent and selective CRBN degrader, classified as a CRBN-VHL hetero-PROTAC. In MM1.S cells, ZXH-4-130 TFA induces approximately 80% CRBN degradation at a concentration of 10 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 1mg, 5mg, 10mg
Package: A1601835
Price: 475, 1330, 2170 (in RMB)
Descriptions: ZXH-4-130 TFA is a highly potent and selective CRBN degrader, classified as a CRBN-VHL hetero-PROTAC. In MM1.S cells, ZXH-4-130 TFA induces approximately 80% CRBN degradation at a concentration of 10 nM.
Last Update: 2026-04-17 13:46:08
CAS: 301-00-8
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 500mg, 1g
Package: A1456329
Price: 472, 693 (in RMB)
Descriptions: Methyl Linolenate is a polyunsaturated fatty acid, used for studying the mechanisms and prevention of unsaturated fatty acid oxidation/peroxidation, with melanogenesis-inhibiting activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 500mg, 1g
Package: A1456329
Price: 472, 693 (in RMB)
Descriptions: Methyl Linolenate is a polyunsaturated fatty acid, used for studying the mechanisms and prevention of unsaturated fatty acid oxidation/peroxidation, with melanogenesis-inhibiting activity.
Last Update: 2026-04-17 13:46:08
CAS: 1176306-10-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1328027
Price: 460, 553, 1104 (in RMB)
Descriptions: Alamandine is a vasoactive peptide, a member of the renin-angiotensin system (RAS), and an endogenous ligand of the G protein-coupled receptor MrgD, protecting the kidneys and heart through its antihypertensive effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A1328027
Price: 460, 553, 1104 (in RMB)
Descriptions: Alamandine is a vasoactive peptide, a member of the renin-angiotensin system (RAS), and an endogenous ligand of the G protein-coupled receptor MrgD, protecting the kidneys and heart through its antihypertensive effects.
Last Update: 2026-04-17 13:46:08
CAS: 7665-99-8
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 25mg
Package: A688624
Price: 455, 1400 (in RMB)
Descriptions: Cyclic GMP is an endogenous second messenger that triggers interferon production in response to cytoplasmic DNA. Cyclic GMP activates the stimulator of interferon genes (STING), activating a signaling cascade that leads to the production of type I interferons and other immune mediators
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 25mg
Package: A688624
Price: 455, 1400 (in RMB)
Descriptions: Cyclic GMP is an endogenous second messenger that triggers interferon production in response to cytoplasmic DNA. Cyclic GMP activates the stimulator of interferon genes (STING), activating a signaling cascade that leads to the production of type I interferons and other immune mediators
Last Update: 2026-04-17 13:46:08
CAS: 3568-90-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A529383
Price: 449, 2970, 840, 2100, 3255 (in RMB)
Descriptions: Deoxylapachol induced fungal cell wall stress and inhibited fungal growth.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A529383
Price: 449, 2970, 840, 2100, 3255 (in RMB)
Descriptions: Deoxylapachol induced fungal cell wall stress and inhibited fungal growth.
Last Update: 2026-04-17 13:46:08
CAS: 125-15-5
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A264401
Price: 454, 1042, 1562 (in RMB)
Descriptions: Vomicine is a natural product isolated and purified from the seeds of Strychnos nux-vomica.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg
Package: A264401
Price: 454, 1042, 1562 (in RMB)
Descriptions: Vomicine is a natural product isolated and purified from the seeds of Strychnos nux-vomica.
Last Update: 2026-04-17 13:46:08
CAS: 1818339-66-0
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A294210
Price: 449, 2926, 958, 2394, 3654 (in RMB)
Descriptions: PF-06751979 is a potent, brain penetrant, β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor with an IC50 of 7.3 nM in BACE1 binding assay.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A294210
Price: 449, 2926, 958, 2394, 3654 (in RMB)
Descriptions: PF-06751979 is a potent, brain penetrant, β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor with an IC50 of 7.3 nM in BACE1 binding assay.
Last Update: 2026-04-17 13:46:08
CAS: 244101-02-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A912792
Price: 447, 983, 1573, 3440, 5529 (in RMB)
Descriptions: L-798106 is a potent and highly selective prostanoid EP3 receptor antagonist (Ki values are 0.3, 916, > 5000 and > 5000 nM at EP3, EP4, EP1 and EP2, respectively), and it can attenuate sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A912792
Price: 447, 983, 1573, 3440, 5529 (in RMB)
Descriptions: L-798106 is a potent and highly selective prostanoid EP3 receptor antagonist (Ki values are 0.3, 916, > 5000 and > 5000 nM at EP3, EP4, EP1 and EP2, respectively), and it can attenuate sulprostone-induced inhibition of EFS-evoked twitch and contractile responses in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 90-19-7
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A554234
Price: 441, 1071, 1701 (in RMB)
Descriptions: Rhamnetin is a quercetin derivative extracted from coriander that inhibits the activity of secretory phospholipase A2, possessing antioxidant and anti-inflammatory properties.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 1mg, 5mg, 10mg
Package: A554234
Price: 441, 1071, 1701 (in RMB)
Descriptions: Rhamnetin is a quercetin derivative extracted from coriander that inhibits the activity of secretory phospholipase A2, possessing antioxidant and anti-inflammatory properties.
Last Update: 2026-04-17 13:46:08
CAS: 1268881-20-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A852916
Price: 429, 945, 1512, 3024, 4914 (in RMB)
Descriptions: Olorinab (APD 371) is a potent and selective full agonist targeting cannabinoid receptor type 2 (CB2), with an EC50 value of 6.2 nM for hCB2.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A852916
Price: 429, 945, 1512, 3024, 4914 (in RMB)
Descriptions: Olorinab (APD 371) is a potent and selective full agonist targeting cannabinoid receptor type 2 (CB2), with an EC50 value of 6.2 nM for hCB2.
Last Update: 2026-04-17 13:46:08
CAS: 1379545-95-5
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A711494
Price: 437, 1090, 1730, 2910 (in RMB)
Descriptions: MSC2363318A, also known as M2698, is an orally available inhibitor of the serine/threonine protein kinases ribosomal protein S6 Kinase (p70S6K) and Akt (protein kinase B), with potential antineoplastic activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A711494
Price: 437, 1090, 1730, 2910 (in RMB)
Descriptions: MSC2363318A, also known as M2698, is an orally available inhibitor of the serine/threonine protein kinases ribosomal protein S6 Kinase (p70S6K) and Akt (protein kinase B), with potential antineoplastic activity.
Last Update: 2026-04-17 13:46:08
CAS: 60482-95-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A725376
Price: 420, 840, 1470, 3080 (in RMB)
Descriptions: Neurotensin Fragment 8-13 is the smallest active fragment of neurotensin which is a potent cellular mitogen for various colorectal and pancreatic cancers which possess high-affinity neurotensin receptors (NTR).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg
Package: A725376
Price: 420, 840, 1470, 3080 (in RMB)
Descriptions: Neurotensin Fragment 8-13 is the smallest active fragment of neurotensin which is a potent cellular mitogen for various colorectal and pancreatic cancers which possess high-affinity neurotensin receptors (NTR).
Last Update: 2026-04-17 13:46:08
CAS: 24063-71-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A987457
Price: 420, 1050, 1680 (in RMB)
Descriptions: Isocurcumenol is a compound isolated from Curcuma zedoaria, which acts as an ERα inhibitor and has anti-tumor activity. Its IC50 values against DLA and KB cancer cells are 99.1 µg/mL and 178.2 µg/mL, respectively, suitable for anti-cancer drug research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A987457
Price: 420, 1050, 1680 (in RMB)
Descriptions: Isocurcumenol is a compound isolated from Curcuma zedoaria, which acts as an ERα inhibitor and has anti-tumor activity. Its IC50 values against DLA and KB cancer cells are 99.1 µg/mL and 178.2 µg/mL, respectively, suitable for anti-cancer drug research.
Last Update: 2026-04-17 13:46:08
CAS: 103188-48-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg
Package: A1274965
Price: 419, 2766, 760, 1510, 1827, 2835 (in RMB)
Descriptions: N-trans-Caffeoyltyramine is an effective modulator of inflammatory responses with antioxidant and anticoagulant properties.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg
Package: A1274965
Price: 419, 2766, 760, 1510, 1827, 2835 (in RMB)
Descriptions: N-trans-Caffeoyltyramine is an effective modulator of inflammatory responses with antioxidant and anticoagulant properties.
Last Update: 2026-04-17 13:46:08
CAS: 37905-08-1
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg
Package: A753189
Price: 420, 1050, 1680 (in RMB)
Descriptions: Jolkinolide B is a bioactive diterpenoid compound isolated from Euphorbia helioscopia, known to induce cancer cell apoptosis and showing significant antitumor activity in colorectal tumors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg
Package: A753189
Price: 420, 1050, 1680 (in RMB)
Descriptions: Jolkinolide B is a bioactive diterpenoid compound isolated from Euphorbia helioscopia, known to induce cancer cell apoptosis and showing significant antitumor activity in colorectal tumors.
Last Update: 2026-04-17 13:46:08
CAS: 1094-08-2
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A724053
Price: 409, 661, 1323 (in RMB)
Descriptions: Ethopropazine HCl is an effective and selective BChE inhibitor with weak inhibition of AChE, a phenothiazine compound with anticholinergic properties useful in Parkinson's disease research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 25mg
Package: A724053
Price: 409, 661, 1323 (in RMB)
Descriptions: Ethopropazine HCl is an effective and selective BChE inhibitor with weak inhibition of AChE, a phenothiazine compound with anticholinergic properties useful in Parkinson's disease research.
Last Update: 2026-04-17 13:46:08
CAS: 119006-77-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg
Package: A701556
Price: 407, 646, 1952 (in RMB)
Descriptions: Flutrimazole is an imidazole antifungal agent with dual anti-inflammatory and antifungal activity. Despite poor transdermal penetration, it shows significant effects in the treatment of localized inflammatory fungal infections.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg
Package: A701556
Price: 407, 646, 1952 (in RMB)
Descriptions: Flutrimazole is an imidazole antifungal agent with dual anti-inflammatory and antifungal activity. Despite poor transdermal penetration, it shows significant effects in the treatment of localized inflammatory fungal infections.
Last Update: 2026-04-17 13:46:08
CAS: 765317-72-4
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A719591
Price: 399, 2626, 552, 1449, 2394 (in RMB)
Descriptions: FRJ is a specific inhibitor of protein tyrosine phosphatase 1B (PTP1B).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A719591
Price: 399, 2626, 552, 1449, 2394 (in RMB)
Descriptions: FRJ is a specific inhibitor of protein tyrosine phosphatase 1B (PTP1B).
Last Update: 2026-04-17 13:46:08
CAS: 220551-92-8
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 2mg, 5mg, 10mg, 25mg, 50mg
Package: A756565
Price: 388, 698, 1187, 1990, 2970 (in RMB)
Descriptions: DAA1106 is a potent and selective ligand for peripheral benzodiazepine receptor (PBR), as a potent and selective agonist at the peripheral benzodiazepine receptor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 2mg, 5mg, 10mg, 25mg, 50mg
Package: A756565
Price: 388, 698, 1187, 1990, 2970 (in RMB)
Descriptions: DAA1106 is a potent and selective ligand for peripheral benzodiazepine receptor (PBR), as a potent and selective agonist at the peripheral benzodiazepine receptor.
Last Update: 2026-04-17 13:46:08
CAS: 2170136-86-2
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1964086
Price: 389, 2522, 859, 1890, 2835 (in RMB)
Descriptions: GSK3735967 is a selective, reversible non-nucleoside DNMT1 inhibitor that contains a planar dicyanopyridine core, specifically embedding into the semi-methylated CpG dinucleotide bound by DNMT1. GSK3735967 has three binding sites, one of which can bind to histone H4K20me3.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Epigenetics
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1964086
Price: 389, 2522, 859, 1890, 2835 (in RMB)
Descriptions: GSK3735967 is a selective, reversible non-nucleoside DNMT1 inhibitor that contains a planar dicyanopyridine core, specifically embedding into the semi-methylated CpG dinucleotide bound by DNMT1. GSK3735967 has three binding sites, one of which can bind to histone H4K20me3.
Last Update: 2026-04-17 13:46:08
CAS: 3733-63-9
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 25mg, 50mg
Package: A114849
Price: 386, 624 (in RMB)
Descriptions: Decloxizine is a histamine 1 receptor antagonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 25mg, 50mg
Package: A114849
Price: 386, 624 (in RMB)
Descriptions: Decloxizine is a histamine 1 receptor antagonist.
Last Update: 2026-04-17 13:46:08
CAS: 1072959-67-1
Category: Inhibitors|Agonists, Cell Cycle
Spec: 5mg, 10mg, 50mg, 100mg
Package: A405951
Price: 378, 630, 2016, 3226 (in RMB)
Descriptions: SR-3677 is a potent and selective ROCK-II inhibitor with an IC50 of ~3 nM in enzyme and cell based assays, and its IC50 for ROCK-I is 56 ± 12 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 5mg, 10mg, 50mg, 100mg
Package: A405951
Price: 378, 630, 2016, 3226 (in RMB)
Descriptions: SR-3677 is a potent and selective ROCK-II inhibitor with an IC50 of ~3 nM in enzyme and cell based assays, and its IC50 for ROCK-I is 56 ± 12 nM.
Last Update: 2026-04-17 13:46:08
CAS: 3301-49-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A165386
Price: 385, 1190 (in RMB)
Descriptions: Kumatakenin, a natural product isolated and purified from the roots of Astragalus membranaceus, has antibacterial and antifungal activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg
Package: A165386
Price: 385, 1190 (in RMB)
Descriptions: Kumatakenin, a natural product isolated and purified from the roots of Astragalus membranaceus, has antibacterial and antifungal activities.
Last Update: 2026-04-17 13:46:08
CAS: 74805-92-8
Category: Natural product, Liliaceae
Spec: 1mg, 5mg, 10mg
Package: A261212
Price: 378, 864, 1330 (in RMB)
Descriptions: Methylophiopogonanone A, a natural product isolated and purified from the roots of Ophiopogon japonicus with anti-inflammatory and anti-oxidative properties, has therapeutic potential against cerebral I/R injury through its ability to attenuate BBB disruption by regulating the expression of MMP-9 and tight junction proteins.
Last Update: 2026-04-17 13:46:08
Category: Natural product, Liliaceae
Spec: 1mg, 5mg, 10mg
Package: A261212
Price: 378, 864, 1330 (in RMB)
Descriptions: Methylophiopogonanone A, a natural product isolated and purified from the roots of Ophiopogon japonicus with anti-inflammatory and anti-oxidative properties, has therapeutic potential against cerebral I/R injury through its ability to attenuate BBB disruption by regulating the expression of MMP-9 and tight junction proteins.
Last Update: 2026-04-17 13:46:08
CAS: 123748-68-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg
Package: A1371128
Price: 369, 2491, 1015, 1523, 4060 (in RMB)
Descriptions: Escin IA is the main active ingredient of the saponin fraction of Aesculus chinensis Bunge fruits (SFAC) for the anti-TNBC metastasis activity, and its action mechanisms involved inhibition of EMT process by down-regulating LOXL2 expression.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg
Package: A1371128
Price: 369, 2491, 1015, 1523, 4060 (in RMB)
Descriptions: Escin IA is the main active ingredient of the saponin fraction of Aesculus chinensis Bunge fruits (SFAC) for the anti-TNBC metastasis activity, and its action mechanisms involved inhibition of EMT process by down-regulating LOXL2 expression.
Last Update: 2026-04-17 13:46:08
CAS: 24268-41-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A448676
Price: 360, 945, 1386 (in RMB)
Descriptions: Furanodienone is one of the primary active components in turmeric rhizomes, exerting its anti-tumor effects through the induction of apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A448676
Price: 360, 945, 1386 (in RMB)
Descriptions: Furanodienone is one of the primary active components in turmeric rhizomes, exerting its anti-tumor effects through the induction of apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 79352-78-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A611996
Price: 359, 2310, 859, 1890, 3465 (in RMB)
Descriptions: N-Desethyl amodiaquine is the bioactive metabolite of Amodiaquine with antiparasitic effects, exhibiting IC50 values of 97 nM and 25 nM against V1/S and 3D7 strains, respectively. It is used in malaria research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A611996
Price: 359, 2310, 859, 1890, 3465 (in RMB)
Descriptions: N-Desethyl amodiaquine is the bioactive metabolite of Amodiaquine with antiparasitic effects, exhibiting IC50 values of 97 nM and 25 nM against V1/S and 3D7 strains, respectively. It is used in malaria research.
Last Update: 2026-04-17 13:46:08
CAS: 135330-08-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1142884
Price: 359, 2379, 542, 1120, 1792, 3248 (in RMB)
Descriptions: RP-54745 is an inhibitor of macrophage stimulation and interleukin-1 production, and a potential antirheumatic compound.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1142884
Price: 359, 2379, 542, 1120, 1792, 3248 (in RMB)
Descriptions: RP-54745 is an inhibitor of macrophage stimulation and interleukin-1 production, and a potential antirheumatic compound.
Last Update: 2026-04-17 13:46:08
CAS: 26544-34-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A101993
Price: 350, 980, 1470, 2499, 3499, 4389 (in RMB)
Descriptions: Apiin can inhibit iNOS expression and nitrite production in J774.A1 cells. It is a flavonoid isolated from the herbs of petroselinum crispum.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A101993
Price: 350, 980, 1470, 2499, 3499, 4389 (in RMB)
Descriptions: Apiin can inhibit iNOS expression and nitrite production in J774.A1 cells. It is a flavonoid isolated from the herbs of petroselinum crispum.
Last Update: 2026-04-17 13:46:08
CAS: 74639-14-8
Category: Natural product, Rhamnaceae
Spec: 5mg, 10mg, 25mg
Package: A217043
Price: 346, 535, 1039 (in RMB)
Descriptions: Liquiritin apioside is a natural product which extracted from glycyrrhiza uralensis.
Last Update: 2026-04-17 13:46:08
Category: Natural product, Rhamnaceae
Spec: 5mg, 10mg, 25mg
Package: A217043
Price: 346, 535, 1039 (in RMB)
Descriptions: Liquiritin apioside is a natural product which extracted from glycyrrhiza uralensis.
Last Update: 2026-04-17 13:46:08
CAS: 23827-91-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg
Package: A1177438
Price: 346, 554, 1197 (in RMB)
Descriptions: [Des-Arg9]-Bradykinin acetate is an agonist for bradykinin B1 receptor with higher selectivity than B2 receptor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg
Package: A1177438
Price: 346, 554, 1197 (in RMB)
Descriptions: [Des-Arg9]-Bradykinin acetate is an agonist for bradykinin B1 receptor with higher selectivity than B2 receptor.
Last Update: 2026-04-17 13:46:08
CAS: 882268-69-1
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1554691
Price: 340, 596, 1180, 2030, 2920 (in RMB)
Descriptions: HIF-2α-IN-4 is a potent HIF-2α translation inhibitor with an IC50 value of 5 μM, capable of inhibiting both constitutive and hypoxia-induced HIF-2α protein expression.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1554691
Price: 340, 596, 1180, 2030, 2920 (in RMB)
Descriptions: HIF-2α-IN-4 is a potent HIF-2α translation inhibitor with an IC50 value of 5 μM, capable of inhibiting both constitutive and hypoxia-induced HIF-2α protein expression.
Last Update: 2026-04-17 13:46:08
CAS: 1369852-71-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1142906
Price: 339, 2274, 731, 1575, 2520, 4725 (in RMB)
Descriptions: Lotilaner is a non-competitive insect GABACl receptor antagonist with an IC50 of 23.84 nM, exhibiting antiparasitic activity and widely used for treating parasitic infections in animals like dogs, with no significant effect on mammalian GABAA receptors.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1142906
Price: 339, 2274, 731, 1575, 2520, 4725 (in RMB)
Descriptions: Lotilaner is a non-competitive insect GABACl receptor antagonist with an IC50 of 23.84 nM, exhibiting antiparasitic activity and widely used for treating parasitic infections in animals like dogs, with no significant effect on mammalian GABAA receptors.
Last Update: 2026-04-17 13:46:08
CAS: 1340593-59-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A449607
Price: 339, 2274, 1764, 2835, 4347 (in RMB)
Descriptions: Oteseconazole (VT-1161) stands out as an effective and orally administered agent against fungi. It strongly attaches to and inhibits the activity of Candida albicans' cytochrome P45051 (CYP51) with a Kd of 39 nM or less, while not affecting human CYP51.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A449607
Price: 339, 2274, 1764, 2835, 4347 (in RMB)
Descriptions: Oteseconazole (VT-1161) stands out as an effective and orally administered agent against fungi. It strongly attaches to and inhibits the activity of Candida albicans' cytochrome P45051 (CYP51) with a Kd of 39 nM or less, while not affecting human CYP51.
Last Update: 2026-04-17 13:46:08
CAS: 2459963-17-6
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A544247
Price: 339, 700, 1120, 2100, 3360 (in RMB)
Descriptions: TP0427736 HCl is the HCl form of TP0427736 which is an inhibitor of ALK5 with IC50 of 2.72 nM and can reduce TGF-β induced growth.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A544247
Price: 339, 700, 1120, 2100, 3360 (in RMB)
Descriptions: TP0427736 HCl is the HCl form of TP0427736 which is an inhibitor of ALK5 with IC50 of 2.72 nM and can reduce TGF-β induced growth.
Last Update: 2026-04-17 13:46:08
CAS: 100986-86-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg
Package: A990574
Price: 336, 560, 1120 (in RMB)
Descriptions: (R)-Ofloxacin (Dextrofloxacin) is an antibiotic used in the research of many bacterial infections. It possesses antibacterial activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg
Package: A990574
Price: 336, 560, 1120 (in RMB)
Descriptions: (R)-Ofloxacin (Dextrofloxacin) is an antibiotic used in the research of many bacterial infections. It possesses antibacterial activity.
Last Update: 2026-04-17 13:46:08
CAS: 916075-84-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549519
Price: 329, 2175, 592, 1530, 2270 (in RMB)
Descriptions: Felcisetrag (TD-8954) is an effective and selective orally active 5-HT4 receptor agonist with prokinetic properties in the gastrointestinal tract. It shows high affinity for the human recombinant 5-HT4(c) (h5-HT4(c)) receptor, with a pKi of 9.4.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549519
Price: 329, 2175, 592, 1530, 2270 (in RMB)
Descriptions: Felcisetrag (TD-8954) is an effective and selective orally active 5-HT4 receptor agonist with prokinetic properties in the gastrointestinal tract. It shows high affinity for the human recombinant 5-HT4(c) (h5-HT4(c)) receptor, with a pKi of 9.4.
Last Update: 2026-04-17 13:46:08
CAS: 56995-20-1
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 10mg, 50mg, 100mg
Package: A456752
Price: 328, 649, 1016 (in RMB)
Descriptions: Flupirtine is a selective neuronal potassium channel opener that also has NMDA receptor antagonist properties.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 10mg, 50mg, 100mg
Package: A456752
Price: 328, 649, 1016 (in RMB)
Descriptions: Flupirtine is a selective neuronal potassium channel opener that also has NMDA receptor antagonist properties.
Last Update: 2026-04-17 13:46:08
CAS: 29331-92-8
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50mg, 100mg
Package: A334944
Price: 315, 441 (in RMB)
Descriptions: Licarbazepine, also known as BIA-2-005; GP-47779; LIC-477; LIC-477D; TRI-477, is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects that is related to oxcarbazepine. It is an active metabolite of oxcarbazepine. In addition, an isomer of licarbazepine, eslicarbazepine ((S)-(+)-licarbazepine), is an active metabolite of eslicarbazepine acetate. Oxcarbazepine and eslicarbazepine acetate are inactive on their own, and behave instead as prodrugs to licarbazepine and eslicarbazepine, respectively, to produce their therapeutic effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 50mg, 100mg
Package: A334944
Price: 315, 441 (in RMB)
Descriptions: Licarbazepine, also known as BIA-2-005; GP-47779; LIC-477; LIC-477D; TRI-477, is a voltage-gated sodium channel blocker with anticonvulsant and mood-stabilizing effects that is related to oxcarbazepine. It is an active metabolite of oxcarbazepine. In addition, an isomer of licarbazepine, eslicarbazepine ((S)-(+)-licarbazepine), is an active metabolite of eslicarbazepine acetate. Oxcarbazepine and eslicarbazepine acetate are inactive on their own, and behave instead as prodrugs to licarbazepine and eslicarbazepine, respectively, to produce their therapeutic effects.
Last Update: 2026-04-17 13:46:08
CAS: 951659-40-8
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 50mg, 100mg
Package: A1256938
Price: 315, 535, 1575, 2520 (in RMB)
Descriptions: Flupyradifurone is a nicotinic acetylcholine receptor (nAChR) agonist that interferes with pest neural signal transmission, making it an effective insecticide.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 5mg, 10mg, 50mg, 100mg
Package: A1256938
Price: 315, 535, 1575, 2520 (in RMB)
Descriptions: Flupyradifurone is a nicotinic acetylcholine receptor (nAChR) agonist that interferes with pest neural signal transmission, making it an effective insecticide.
Last Update: 2026-04-17 13:46:08
CAS: 1613509-49-1
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1550788
Price: 315, 693, 1134, 2268, 3654, 5985 (in RMB)
Descriptions: SRI-41315 induces prolonged stalling of stop codons, inhibiting premature termination codons (PTCs) associated with cystic fibrosis and restoring CFTR protein expression and function. By reducing the abundance of termination factor eRF1 while enhancing aminoglycoside-mediated readthrough, SRI-41315 significantly increases CFTR activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1550788
Price: 315, 693, 1134, 2268, 3654, 5985 (in RMB)
Descriptions: SRI-41315 induces prolonged stalling of stop codons, inhibiting premature termination codons (PTCs) associated with cystic fibrosis and restoring CFTR protein expression and function. By reducing the abundance of termination factor eRF1 while enhancing aminoglycoside-mediated readthrough, SRI-41315 significantly increases CFTR activity.
Last Update: 2026-04-17 13:46:08
CAS: 2035814-50-5
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1149111
Price: 309, 2049, 777, 2100, 3080, 5443 (in RMB)
Descriptions: JNJ-61432059 is an oral active and selective negative modulator of AMPAR associated with trans-membrane AMPAR regulatory protein (TARP) γ-8, with a pIC50 of 9.7 for GluA1/γ-8. Exhibits time- and dose-dependent AMPAR/γ-8 receptor occupancy in mouse hippocampus, resulting in robust seizure protection in corneal kindling and pentylenetetrazole (PTZ) anticonvulsant models[1].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Neuronal Signaling
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A1149111
Price: 309, 2049, 777, 2100, 3080, 5443 (in RMB)
Descriptions: JNJ-61432059 is an oral active and selective negative modulator of AMPAR associated with trans-membrane AMPAR regulatory protein (TARP) γ-8, with a pIC50 of 9.7 for GluA1/γ-8. Exhibits time- and dose-dependent AMPAR/γ-8 receptor occupancy in mouse hippocampus, resulting in robust seizure protection in corneal kindling and pentylenetetrazole (PTZ) anticonvulsant models[1].
Last Update: 2026-04-17 13:46:08
CAS: 1229453-99-9
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1145660
Price: 299, 1929, 784, 1960, 3024 (in RMB)
Descriptions: Acrizanib is a selective VEGFR2 inhibitor with IC50 value of 17.4nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1145660
Price: 299, 1929, 784, 1960, 3024 (in RMB)
Descriptions: Acrizanib is a selective VEGFR2 inhibitor with IC50 value of 17.4nM.
Last Update: 2026-04-17 13:46:08
CAS: 23694-17-9
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A279692
Price: 294, 560, 840, 1680, 2520 (in RMB)
Descriptions: Sultopride HCl is a selective antagonist of dopamine D2 receptor
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A279692
Price: 294, 560, 840, 1680, 2520 (in RMB)
Descriptions: Sultopride HCl is a selective antagonist of dopamine D2 receptor
Last Update: 2026-04-17 13:46:08
CAS: 110505-75-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 50mg, 100mg
Package: A163624
Price: 294, 490, 1680, 2800 (in RMB)
Descriptions: N6-(4-Hydroxybenzyl)adenosine is an inhibitor of platelet aggregation induced in vitro by collagen and their activity range was demonstrated (IC50: 6.77-141 μM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 50mg, 100mg
Package: A163624
Price: 294, 490, 1680, 2800 (in RMB)
Descriptions: N6-(4-Hydroxybenzyl)adenosine is an inhibitor of platelet aggregation induced in vitro by collagen and their activity range was demonstrated (IC50: 6.77-141 μM).
Last Update: 2026-04-17 13:46:08
CAS: 52012-29-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A498495
Price: 289, 663, 968 (in RMB)
Descriptions: Isoschaftoside is a natural product isolated and purified from the herbs of Desmodium styracifolium (Osh.) Merr. with antioxidant and anticancer activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A498495
Price: 289, 663, 968 (in RMB)
Descriptions: Isoschaftoside is a natural product isolated and purified from the herbs of Desmodium styracifolium (Osh.) Merr. with antioxidant and anticancer activities.
Last Update: 2026-04-17 13:46:08
CAS: 204326-43-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A383759
Price: 293, 653, 1090 (in RMB)
Descriptions: NS-2028 is a potent soluble guanylyl cyclase (sGC) inhibitor with Ki of 8 nM. NS-2028 inhibits sGC activity in homogenates of mouse cerebellum and neuronal NO synthase with IC50 values of 17 nM and 20 nM[1]. NS-2028 is commonly used in the research of nitric oxide signaling pathways, it inhibits NO-dependent relaxant responses in non-vascular smooth muscle completely (1 μM)[1]. NS-2028 reduces vascular endothelial growth factor-induced angiogenesis and permeability[2].
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg
Package: A383759
Price: 293, 653, 1090 (in RMB)
Descriptions: NS-2028 is a potent soluble guanylyl cyclase (sGC) inhibitor with Ki of 8 nM. NS-2028 inhibits sGC activity in homogenates of mouse cerebellum and neuronal NO synthase with IC50 values of 17 nM and 20 nM[1]. NS-2028 is commonly used in the research of nitric oxide signaling pathways, it inhibits NO-dependent relaxant responses in non-vascular smooth muscle completely (1 μM)[1]. NS-2028 reduces vascular endothelial growth factor-induced angiogenesis and permeability[2].
Last Update: 2026-04-17 13:46:08
CAS: 929915-58-2
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A385038
Price: 286, 696, 1190, 2530, 3520 (in RMB)
Descriptions: DG051 is a potent leukotriene A4 hydrolase inhibitor of leukotriene B4 biosynthesis in the enzyme assay with an IC50=47 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A385038
Price: 286, 696, 1190, 2530, 3520 (in RMB)
Descriptions: DG051 is a potent leukotriene A4 hydrolase inhibitor of leukotriene B4 biosynthesis in the enzyme assay with an IC50=47 nM.
Last Update: 2026-04-17 13:46:08
CAS: 166977-43-1
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A627846
Price: 287, 678, 1180, 1980, 2920 (in RMB)
Descriptions: BMS453 (BMS-189453) is a synthetic vitamin A analog with RARβ agonist activity and RARα/RARγ antagonistic activity. It primarily inhibits mammary cell growth by inducing active TGFβ.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Vitamin D related|nuclear receptor
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A627846
Price: 287, 678, 1180, 1980, 2920 (in RMB)
Descriptions: BMS453 (BMS-189453) is a synthetic vitamin A analog with RARβ agonist activity and RARα/RARγ antagonistic activity. It primarily inhibits mammary cell growth by inducing active TGFβ.
Last Update: 2026-04-17 13:46:08
CAS: 2244684-49-7
Category: PROTAC, PROTAC Molecule
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1147984
Price: 287, 644, 840, 1680, 2453, 3521 (in RMB)
Descriptions: CM11 is a PROTAC with VHL ligand and targeting on VHL self-degradation with DC50<100nM.
Last Update: 2026-04-17 13:46:08
Category: PROTAC, PROTAC Molecule
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1147984
Price: 287, 644, 840, 1680, 2453, 3521 (in RMB)
Descriptions: CM11 is a PROTAC with VHL ligand and targeting on VHL self-degradation with DC50<100nM.
Last Update: 2026-04-17 13:46:08
CAS: 426834-69-7
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A1159096
Price: 283, 738, 1170 (in RMB)
Descriptions: NS5806, a KV4.3 channel activator, increases peak current amplitude of the potassium channel Kv4.3 with EC50 of 5.3 uM. NS5806 also slows Kv4.3 and Kv4.2 current dacay in channel complexes containing KChIP2.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg
Package: A1159096
Price: 283, 738, 1170 (in RMB)
Descriptions: NS5806, a KV4.3 channel activator, increases peak current amplitude of the potassium channel Kv4.3 with EC50 of 5.3 uM. NS5806 also slows Kv4.3 and Kv4.2 current dacay in channel complexes containing KChIP2.
Last Update: 2026-04-17 13:46:08
CAS: 26807-65-8
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 500mg, 1g, 5g
Package: A706185
Price: 280, 350, 573 (in RMB)
Descriptions: Indapamide is a thiazide sulphonamide diuretic compound, generally used in the treatment of hypertension, as well as decompensated cardiac failure.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 500mg, 1g, 5g
Package: A706185
Price: 280, 350, 573 (in RMB)
Descriptions: Indapamide is a thiazide sulphonamide diuretic compound, generally used in the treatment of hypertension, as well as decompensated cardiac failure.
Last Update: 2026-04-17 13:46:08
CAS: 131926-99-3
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg
Package: A554989
Price: 280, 700, 1120, 2240 (in RMB)
Descriptions: Lansoprazole sulfone (AG-1813) is an orally active and selective H+, K+-ATPase inhibitor. Lansoprazole sulfone significantly stimulates gastric acid secretion by inhibiting H+, K+-ATPase. It has potential applications in duodenal ulcers, gastric ulcers, gastroesophageal reflux disease, and Zollinger-Ellison syndrome.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg
Package: A554989
Price: 280, 700, 1120, 2240 (in RMB)
Descriptions: Lansoprazole sulfone (AG-1813) is an orally active and selective H+, K+-ATPase inhibitor. Lansoprazole sulfone significantly stimulates gastric acid secretion by inhibiting H+, K+-ATPase. It has potential applications in duodenal ulcers, gastric ulcers, gastroesophageal reflux disease, and Zollinger-Ellison syndrome.
Last Update: 2026-04-17 13:46:08
CAS: 2415225-30-6
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1515552
Price: 279, 1866, 916, 2016, 3213 (in RMB)
Descriptions: Acid Ceramidase-IN-1 is an effective orally bioavailable inhibitor of acid sphingomyelinase (ASAH-1), with an IC50 of 0.166 μM. This compound has good brain penetrability and is suitable for research on neurodegenerative diseases and other disorders related to ceramide metabolism.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1515552
Price: 279, 1866, 916, 2016, 3213 (in RMB)
Descriptions: Acid Ceramidase-IN-1 is an effective orally bioavailable inhibitor of acid sphingomyelinase (ASAH-1), with an IC50 of 0.166 μM. This compound has good brain penetrability and is suitable for research on neurodegenerative diseases and other disorders related to ceramide metabolism.
Last Update: 2026-04-17 13:46:08
CAS: 1361224-53-4
Category: Inhibitors|Agonists, Classical Positive Drug
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A491672
Price: 279, 1867, 493, 1150, 1630, 3670 (in RMB)
Descriptions: AMG-3969 is a glucokinase-GKRP disruptor with IC50 value of 343nM and potently reverses the inhibitory effect of GKRP on GK activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Classical Positive Drug
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg
Package: A491672
Price: 279, 1867, 493, 1150, 1630, 3670 (in RMB)
Descriptions: AMG-3969 is a glucokinase-GKRP disruptor with IC50 value of 343nM and potently reverses the inhibitory effect of GKRP on GK activity.
Last Update: 2026-04-17 13:46:08
CAS: 1799948-06-3
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A100621
Price: 279, 1873, 805, 2100, 3360 (in RMB)
Descriptions: HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A100621
Price: 279, 1873, 805, 2100, 3360 (in RMB)
Descriptions: HIF-2α-IN-1 is a HIF-2α inhibitor has an IC50 of less than 500 nM in HIF-2α scintillation proximity assay.
Last Update: 2026-04-17 13:46:08
CAS: 65995-64-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A962560
Price: 277, 756, 1260 (in RMB)
Descriptions: Punicalincan be extracted from pomegranate leaves, has anti-hepatitis B virus (HBV) activity, and acts by inducing pyroptosis. In addition, Punicalin can inhibit carbonic anhydrase and prevent S-glycoprotein from binding to ACE2 receptors, which has anti-inflammatory, antioxidant and antiviral activities.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg
Package: A962560
Price: 277, 756, 1260 (in RMB)
Descriptions: Punicalincan be extracted from pomegranate leaves, has anti-hepatitis B virus (HBV) activity, and acts by inducing pyroptosis. In addition, Punicalin can inhibit carbonic anhydrase and prevent S-glycoprotein from binding to ACE2 receptors, which has anti-inflammatory, antioxidant and antiviral activities.
Last Update: 2026-04-17 13:46:08
CAS: 154563-54-9
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1193879
Price: 277, 672, 1090, 1780, 2740 (in RMB)
Descriptions: SP-100030 is a dual inhibitor of NF-κB and AP-1 with an IC50 of 50 nM for both, inhibiting IL-2, IL-8, and TNF-α production in Jurkat and other T cell lines and reducing symptoms in a mouse model of collagen-induced arthritis (CIA).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, NF-κB Signaling Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1193879
Price: 277, 672, 1090, 1780, 2740 (in RMB)
Descriptions: SP-100030 is a dual inhibitor of NF-κB and AP-1 with an IC50 of 50 nM for both, inhibiting IL-2, IL-8, and TNF-α production in Jurkat and other T cell lines and reducing symptoms in a mouse model of collagen-induced arthritis (CIA).
Last Update: 2026-04-17 13:46:08
CAS: 1268882-43-4
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A891114
Price: 273, 596, 893, 1590, 2210 (in RMB)
Descriptions: MK 1903 is a potent and selective hydroxycarboxylic acid receptor 2 (HCA2, GPR109A) full agonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A891114
Price: 273, 596, 893, 1590, 2210 (in RMB)
Descriptions: MK 1903 is a potent and selective hydroxycarboxylic acid receptor 2 (HCA2, GPR109A) full agonist.
Last Update: 2026-04-17 13:46:08
CAS: 1269826-44-9
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1532017
Price: 269, 1712, 1680, 2660, 5160, 6930 (in RMB)
Descriptions: OSBPL7-IN-1 is an OSBPL7 (Oxysterol-binding protein-like 7) inhibitor used to study lipid metabolism, cell signaling, and related diseases such as cardiovascular diseases and metabolic syndrome.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1532017
Price: 269, 1712, 1680, 2660, 5160, 6930 (in RMB)
Descriptions: OSBPL7-IN-1 is an OSBPL7 (Oxysterol-binding protein-like 7) inhibitor used to study lipid metabolism, cell signaling, and related diseases such as cardiovascular diseases and metabolic syndrome.
Last Update: 2026-04-17 13:46:08
CAS: 62956-48-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A133513
Price: 269, 1736, 504, 1323, 2079 (in RMB)
Descriptions: Gomisin G is an ethanolic extract of the stems of Kadsura interior and exhibits potent anti-HIV activity with EC50 and therapeutic index (TI) values of 0.006 mg/mL and 300, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A133513
Price: 269, 1736, 504, 1323, 2079 (in RMB)
Descriptions: Gomisin G is an ethanolic extract of the stems of Kadsura interior and exhibits potent anti-HIV activity with EC50 and therapeutic index (TI) values of 0.006 mg/mL and 300, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 4846-19-9
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A861174
Price: 269, 1771, 881, 1449, 2489 (in RMB)
Descriptions: N-Nornuciferine, a natural product isolated and purified from the fruits of Piper nigrum, can competitively inhibit CYP2D6 activity with Ki values of 2.34 uM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A861174
Price: 269, 1771, 881, 1449, 2489 (in RMB)
Descriptions: N-Nornuciferine, a natural product isolated and purified from the fruits of Piper nigrum, can competitively inhibit CYP2D6 activity with Ki values of 2.34 uM.
Last Update: 2026-04-17 13:46:08
CAS: 1398609-39-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1142904
Price: 266, 700, 1120, 2345, 3780 (in RMB)
Descriptions: Sarolaner is an orally active isoxazoline compound widely used to control ectoparasites (e.g., fleas and ticks), exhibiting high inhibitory activity against C. felis and O. turicata with LC80 and LC100 values of 0.3 μg/mL and 0.003 μg/mL, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1142904
Price: 266, 700, 1120, 2345, 3780 (in RMB)
Descriptions: Sarolaner is an orally active isoxazoline compound widely used to control ectoparasites (e.g., fleas and ticks), exhibiting high inhibitory activity against C. felis and O. turicata with LC80 and LC100 values of 0.3 μg/mL and 0.003 μg/mL, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 1421373-62-7
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 50mg
Package: A410986
Price: 260, 646, 864, 2424 (in RMB)
Descriptions: Mutant EGFR inhibitor is a selective and potent Mutated EGFR inhibitor (L858R activating mutant, the Exonl9 deletion activating mutant and the T790M resistance mutant).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 1mg, 5mg, 10mg, 50mg
Package: A410986
Price: 260, 646, 864, 2424 (in RMB)
Descriptions: Mutant EGFR inhibitor is a selective and potent Mutated EGFR inhibitor (L858R activating mutant, the Exonl9 deletion activating mutant and the T790M resistance mutant).
Last Update: 2026-04-17 13:46:08
CAS: 2167246-24-2
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1496588
Price: 251, 620, 980, 1987, 2949 (in RMB)
Descriptions: Rimtuzalcap is a modulator of small-conductance calcium-activated potassium channels.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Membrane Transporter|Ion Channel
Spec: 1mg, 5mg, 10mg, 25mg, 50mg
Package: A1496588
Price: 251, 620, 980, 1987, 2949 (in RMB)
Descriptions: Rimtuzalcap is a modulator of small-conductance calcium-activated potassium channels.
Last Update: 2026-04-17 13:46:08
CAS: 1849603-72-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1216662
Price: 249, 1680, 598, 1386, 2016, 3402, 4725, 5985 (in RMB)
Descriptions: SBI-553 is a potent, brain-penetrant and allosteric modulator of NTR1 with EC50 of 0.34 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A1216662
Price: 249, 1680, 598, 1386, 2016, 3402, 4725, 5985 (in RMB)
Descriptions: SBI-553 is a potent, brain-penetrant and allosteric modulator of NTR1 with EC50 of 0.34 μM.
Last Update: 2026-04-17 13:46:08
CAS: 63302-99-8
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 100mg, 500mg
Package: A793398
Price: 249, 1690, 750, 1805 (in RMB)
Descriptions: Pipofezine is a potent inhibitor of the reuptake of serotonin.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 50μL, 1mL, 100mg, 500mg
Package: A793398
Price: 249, 1690, 750, 1805 (in RMB)
Descriptions: Pipofezine is a potent inhibitor of the reuptake of serotonin.
Last Update: 2026-04-17 13:46:08
CAS: 21411-53-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A219308
Price: 249, 1637, 644, 1415, 2123, 3606 (in RMB)
Descriptions: Virginiamycin M1 (Pristinamycin IIA) is a polyunsaturated macrolide antibiotic produced by Streptomyces virginiae, exhibiting antibacterial activity with a minimum inhibitory concentration (MIC) of 0.25 μg/mL against Staphylococcus aureus. It is commonly used in research against Gram-positive bacterial infections.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A219308
Price: 249, 1637, 644, 1415, 2123, 3606 (in RMB)
Descriptions: Virginiamycin M1 (Pristinamycin IIA) is a polyunsaturated macrolide antibiotic produced by Streptomyces virginiae, exhibiting antibacterial activity with a minimum inhibitory concentration (MIC) of 0.25 μg/mL against Staphylococcus aureus. It is commonly used in research against Gram-positive bacterial infections.
Last Update: 2026-04-17 13:46:08
CAS: 1229024-78-5
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549967
Price: 249, 1684, 1002, 2205, 3654 (in RMB)
Descriptions: TLR7 agonist 3 is a potent Toll-like receptor 7 (TLR7) agonist. TLR7 plays a critical role in immune activation and can be used for the development of immune modulators.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A1549967
Price: 249, 1684, 1002, 2205, 3654 (in RMB)
Descriptions: TLR7 agonist 3 is a potent Toll-like receptor 7 (TLR7) agonist. TLR7 plays a critical role in immune activation and can be used for the development of immune modulators.
Last Update: 2026-04-17 13:46:08
CAS: 67884-30-4
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A287683
Price: 249, 1694, 703, 1386, 2205 (in RMB)
Descriptions: Gigantol is a bibenzyl compound derived from several medicinal orchids. Giganto shows promising therapeutic potential against cancer cells. Gigantol is a novel inhibitor of the Wnt/β-catenin pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A287683
Price: 249, 1694, 703, 1386, 2205 (in RMB)
Descriptions: Gigantol is a bibenzyl compound derived from several medicinal orchids. Giganto shows promising therapeutic potential against cancer cells. Gigantol is a novel inhibitor of the Wnt/β-catenin pathway.
Last Update: 2026-04-17 13:46:08
CAS: 143807-66-3
Category: Inhibitors|Agonists, Pesticide Composition
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A413638
Price: 248, 385, 693, 1120, 3304 (in RMB)
Descriptions: Chromafenozide is a lepidopteran insecticide and it is highly effective in controlling various lepidopteran pests.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Pesticide Composition
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A413638
Price: 248, 385, 693, 1120, 3304 (in RMB)
Descriptions: Chromafenozide is a lepidopteran insecticide and it is highly effective in controlling various lepidopteran pests.
Last Update: 2026-04-17 13:46:08
CAS: 328232-95-7
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 50mg, 100mg
Package: A669432
Price: 247, 596, 942, 2570, 3580 (in RMB)
Descriptions: MK-0557 is a highly selective, orally available neuropeptide Y5 receptor antagonist with a Ki of 1.6 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 50mg, 100mg
Package: A669432
Price: 247, 596, 942, 2570, 3580 (in RMB)
Descriptions: MK-0557 is a highly selective, orally available neuropeptide Y5 receptor antagonist with a Ki of 1.6 nM.
Last Update: 2026-04-17 13:46:08
CAS: 192718-06-2
Category: Inhibitors|Agonists, Ubiquitin
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A280375
Price: 240, 400, 720, 1200, 1840 (in RMB)
Descriptions: C527 is a is a pan DUB enzyme inhibitor, with a high potency for the USP1/UAF1 complex (IC50=0.88 μM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A280375
Price: 240, 400, 720, 1200, 1840 (in RMB)
Descriptions: C527 is a is a pan DUB enzyme inhibitor, with a high potency for the USP1/UAF1 complex (IC50=0.88 μM).
Last Update: 2026-04-17 13:46:08
CAS: 40732-48-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 10mg
Package: A435375
Price: 245, 350 (in RMB)
Descriptions: Cyclic GMP sodium (cGMP) is an important regulator of short-term changes in smooth muscle tone and long-term responses to chronic drug studies or proliferative signals.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 5mg, 10mg
Package: A435375
Price: 245, 350 (in RMB)
Descriptions: Cyclic GMP sodium (cGMP) is an important regulator of short-term changes in smooth muscle tone and long-term responses to chronic drug studies or proliferative signals.
Last Update: 2026-04-17 13:46:08
CAS: 496794-70-8
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A619601
Price: 239, 1589, 485, 1442, 2520, 4031, 4851 (in RMB)
Descriptions: HhAntag is a small molecule inhibitor of GLI1-mediated transcription, an essential down-stream element of the Hedgehog (Hh) pathway, and is an antitumor agent.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A619601
Price: 239, 1589, 485, 1442, 2520, 4031, 4851 (in RMB)
Descriptions: HhAntag is a small molecule inhibitor of GLI1-mediated transcription, an essential down-stream element of the Hedgehog (Hh) pathway, and is an antitumor agent.
Last Update: 2026-04-17 13:46:08
CAS: 2762617-31-0
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A1671310
Price: 239, 1503, 1575, 2394, 4725 (in RMB)
Descriptions: YAP/TAZ inhibitor-2 is a potent TEAD-YAP/TAZ inhibitor with oral bioactivity and an EC50 of 3 nM, capable of inhibiting tumor cell proliferation and showing anti-tumor activity. This compound can be used to study YAP/TAZ-mediated tumor-associated pathways.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 5mg, 10mg, 25mg
Package: A1671310
Price: 239, 1503, 1575, 2394, 4725 (in RMB)
Descriptions: YAP/TAZ inhibitor-2 is a potent TEAD-YAP/TAZ inhibitor with oral bioactivity and an EC50 of 3 nM, capable of inhibiting tumor cell proliferation and showing anti-tumor activity. This compound can be used to study YAP/TAZ-mediated tumor-associated pathways.
Last Update: 2026-04-17 13:46:08
CAS: 2930378-91-7
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1551685
Price: 239, 1540, 1036, 1743, 2863, 4018 (in RMB)
Descriptions: GAK inhibitor 49 hydrochloride is a highly selective inhibitor of cyclin G-associated kinase (GAK, Ki = 0.54 nM, cellular IC50 = 56 nM). It inhibits GAK activity by competing for ATP binding and also interacts with RIPK2, potentially useful for antiviral or neurodegenerative disease research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Protein Tyrosine Kinase|RTK
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A1551685
Price: 239, 1540, 1036, 1743, 2863, 4018 (in RMB)
Descriptions: GAK inhibitor 49 hydrochloride is a highly selective inhibitor of cyclin G-associated kinase (GAK, Ki = 0.54 nM, cellular IC50 = 56 nM). It inhibits GAK activity by competing for ATP binding and also interacts with RIPK2, potentially useful for antiviral or neurodegenerative disease research.
Last Update: 2026-04-17 13:46:08
CAS: 2086809-58-5
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1549733
Price: 239, 1502, 700, 1707, 2739, 5130 (in RMB)
Descriptions: SRI-29329 is a specific CLK inhibitor with IC50 values of 78 nM, 16 nM, and 86 nM for CLK1, CLK2, and CLK4, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A1549733
Price: 239, 1502, 700, 1707, 2739, 5130 (in RMB)
Descriptions: SRI-29329 is a specific CLK inhibitor with IC50 values of 78 nM, 16 nM, and 86 nM for CLK1, CLK2, and CLK4, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 23567-23-9
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A616576
Price: 239, 1515, 346, 1071, 1701 (in RMB)
Descriptions: Cercosporamide is a potent and selective Mnk inhibitor, and an orally bioavailable antifungal agent, suppresses phosphorylation of eIF4E and exhibits antileukemic effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A616576
Price: 239, 1515, 346, 1071, 1701 (in RMB)
Descriptions: Cercosporamide is a potent and selective Mnk inhibitor, and an orally bioavailable antifungal agent, suppresses phosphorylation of eIF4E and exhibits antileukemic effects.
Last Update: 2026-04-17 13:46:08
CAS: 34118-92-8
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg
Package: A989830
Price: 238, 383 (in RMB)
Descriptions: N-Acetylprocainamide HCl is a third-generation antiarrhythmic agent that inhibits potassium channels (K+ channels).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Other Inhibitors|Agonists
Spec: 5mg, 10mg
Package: A989830
Price: 238, 383 (in RMB)
Descriptions: N-Acetylprocainamide HCl is a third-generation antiarrhythmic agent that inhibits potassium channels (K+ channels).
Last Update: 2026-04-17 13:46:08
CAS: 110025-28-0
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg, 100mg
Package: A155352
Price: 229, 380, 1272, 2035 (in RMB)
Descriptions: Endoxifen is a key active metabolite of tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 50mg, 100mg
Package: A155352
Price: 229, 380, 1272, 2035 (in RMB)
Descriptions: Endoxifen is a key active metabolite of tamoxifen (TAM) with higher affinity and specificity to estrogen receptor that also inhibits aromatase activity.
Last Update: 2026-04-17 13:46:08
CAS: 30123-17-2
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 10mg, 50mg, 100mg
Package: A165989
Price: 224, 427, 560 (in RMB)
Descriptions: Tianeptine sodium salt is a selective facilitator of 5-HT uptake in vitro and in vivo.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 10mg, 50mg, 100mg
Package: A165989
Price: 224, 427, 560 (in RMB)
Descriptions: Tianeptine sodium salt is a selective facilitator of 5-HT uptake in vitro and in vivo.
Last Update: 2026-04-17 13:46:08
CAS: 26581-81-7
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1429509
Price: 224, 364, 700, 1015 (in RMB)
Descriptions: 2-(2,6-Dioxopiperidin-3-yl)phthalimidine (EM-12) is a teratogenic thalidomide analog with stronger activity and better hydrolytic stability, enhancing the induction of colon cancer in rats by 1,2-dimethylhydrazine.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 5mg, 10mg, 25mg, 50mg
Package: A1429509
Price: 224, 364, 700, 1015 (in RMB)
Descriptions: 2-(2,6-Dioxopiperidin-3-yl)phthalimidine (EM-12) is a teratogenic thalidomide analog with stronger activity and better hydrolytic stability, enhancing the induction of colon cancer in rats by 1,2-dimethylhydrazine.
Last Update: 2026-04-17 13:46:08
Prodcuts in stock
CAS: 846557-71-9
Category: Cancer
Spec: A722849
Package: 1mg, 5mg, 10mg, 25mg
Price: 119, 591, 189, 472, 819, 1512 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-03 11:26:53
Category: Cancer
Spec: A722849
Package: 1mg, 5mg, 10mg, 25mg
Price: 119, 591, 189, 472, 819, 1512 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-03 11:26:53
CAS: 129497-78-5
Category: Cancer
Spec: A138297
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg
Price: 169, 908, 216, 624, 958 (in RMB)
Descriptions: Verteporfin is a YAP inhibitor, which effectively destroys the YAP-TEAD interaction and induces cell apoptosis. At the same time, as an autophagy inhibitor, it specifically blocks the early stage of autophagy by preventing the formation of autophagy. Verteporfin, as a photosensitizer, can generate reactive oxygen species under illumination, and its IC50 value is 0.6nM. Verteporfin has anti-tumor and anti-angiogenesis effects, and can be used for photodynamic therapy and age-related macular degeneration.
Last Update: 2026-04-03 11:26:53
Category: Cancer
Spec: A138297
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg
Price: 169, 908, 216, 624, 958 (in RMB)
Descriptions: Verteporfin is a YAP inhibitor, which effectively destroys the YAP-TEAD interaction and induces cell apoptosis. At the same time, as an autophagy inhibitor, it specifically blocks the early stage of autophagy by preventing the formation of autophagy. Verteporfin, as a photosensitizer, can generate reactive oxygen species under illumination, and its IC50 value is 0.6nM. Verteporfin has anti-tumor and anti-angiogenesis effects, and can be used for photodynamic therapy and age-related macular degeneration.
Last Update: 2026-04-03 11:26:53
CAS: 518048-05-0
Category: Inhibitors|Agonists
Spec: A121488
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg
Price: 119, 539, 223, 490, 820 (in RMB)
Descriptions: Raltegravir is a powerful integrase (IN) inhibitor used for HIV infection treatment.
Last Update: 2026-04-17 13:49:09
Category: Inhibitors|Agonists
Spec: A121488
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg
Price: 119, 539, 223, 490, 820 (in RMB)
Descriptions: Raltegravir is a powerful integrase (IN) inhibitor used for HIV infection treatment.
Last Update: 2026-04-17 13:49:09
CAS: 915087-33-1
Category: Inhibitors|Agonists
Spec: A270395
Package: 10mM*1mL, 1mg, 5mg, 10mg, 25mg
Price: 693, 233, 408, 656, 1541 (in RMB)
Descriptions: Enzalutamide (MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. It also activates autophagy.
Last Update: 2026-04-17 13:49:09
Category: Inhibitors|Agonists
Spec: A270395
Package: 10mM*1mL, 1mg, 5mg, 10mg, 25mg
Price: 693, 233, 408, 656, 1541 (in RMB)
Descriptions: Enzalutamide (MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. It also activates autophagy.
Last Update: 2026-04-17 13:49:09
CAS: 254750-02-2
Category: Inhibitors|Agonists
Spec: A622861
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Price: 169, 965, 308, 770, 1260, 1995, 2695, 4165 (in RMB)
Descriptions: Emricasan (PF 03491390) is an orally active and irreversible pan-caspase inhibitor that inhibits Zika virus (ZIKV)-induced increases in caspase-3 activity and protects human cortical neural progenitors.
Last Update: 2026-04-17 13:49:09
Category: Inhibitors|Agonists
Spec: A622861
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Price: 169, 965, 308, 770, 1260, 1995, 2695, 4165 (in RMB)
Descriptions: Emricasan (PF 03491390) is an orally active and irreversible pan-caspase inhibitor that inhibits Zika virus (ZIKV)-induced increases in caspase-3 activity and protects human cortical neural progenitors.
Last Update: 2026-04-17 13:49:09
CAS: 755038-65-4
Category: Inhibitors|Agonists
Spec: A232139
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Price: 139, 781, 214, 517, 819, 1894, 2362, 3276 (in RMB)
Descriptions: Volasertib (BI 6727) is an orally active, highly potent, and ATP-competitive inhibitor of Polo-like kinase 1 (PLK1) with an IC50 of 0.87 nM. It inhibits PLK2 and PLK3 with IC50 values of 5 nM and 56 nM, respectively, inducing mitotic arrest and apoptosis. Volasertib, a dihydropteridinone derivative, exhibits significant antitumor activity in various cancer models.
Last Update: 2026-04-17 13:49:09
Category: Inhibitors|Agonists
Spec: A232139
Package: 10mM*50μL, 10mM*1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Price: 139, 781, 214, 517, 819, 1894, 2362, 3276 (in RMB)
Descriptions: Volasertib (BI 6727) is an orally active, highly potent, and ATP-competitive inhibitor of Polo-like kinase 1 (PLK1) with an IC50 of 0.87 nM. It inhibits PLK2 and PLK3 with IC50 values of 5 nM and 56 nM, respectively, inducing mitotic arrest and apoptosis. Volasertib, a dihydropteridinone derivative, exhibits significant antitumor activity in various cancer models.
Last Update: 2026-04-17 13:49:09
CAS: 133407-82-6
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A181909
Price: 109, 353, 220, 296, 630, 976, 1701, 4330 (in RMB)
Descriptions: MG-132 is a peptide aldehyde proteasome inhibitor (IC50=100nM). MG-132 can selectively inhibit chymotrypsin-like activity and Ubiquitin-Proteasome degradation pathway (UPS) of proteasome by binding to the substrate binding site of proteasome, prevent the degradation of Ubiquitin protein, and induce apoptosis, autophagy and anti-inflammatory reaction.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A181909
Price: 109, 353, 220, 296, 630, 976, 1701, 4330 (in RMB)
Descriptions: MG-132 is a peptide aldehyde proteasome inhibitor (IC50=100nM). MG-132 can selectively inhibit chymotrypsin-like activity and Ubiquitin-Proteasome degradation pathway (UPS) of proteasome by binding to the substrate binding site of proteasome, prevent the degradation of Ubiquitin protein, and induce apoptosis, autophagy and anti-inflammatory reaction.
Last Update: 2026-04-17 13:46:08
CAS: 347174-05-4
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A228648
Price: 119, 508, 179, 416, 725, 1544, 2646, 3969 (in RMB)
Descriptions: Ferrostatin-1 is a ferroptosis inhibitor with an IC50 value of 60 nM. Ferrostatin-1 has neuroprotective and antitumor effects and can be used in research on the role of ferroptosis in neurodegenerative diseases and cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A228648
Price: 119, 508, 179, 416, 725, 1544, 2646, 3969 (in RMB)
Descriptions: Ferrostatin-1 is a ferroptosis inhibitor with an IC50 value of 60 nM. Ferrostatin-1 has neuroprotective and antitumor effects and can be used in research on the role of ferroptosis in neurodegenerative diseases and cancer.
Last Update: 2026-04-17 13:46:08
CAS: 53123-88-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A656002
Price: 109, 424, 216, 346, 472, 693, 945, 1572, 2394, 3724 (in RMB)
Descriptions: Rapamycin is a specific mTOR inhibitor with IC50 of ~0.1 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A656002
Price: 109, 424, 216, 346, 472, 693, 945, 1572, 2394, 3724 (in RMB)
Descriptions: Rapamycin is a specific mTOR inhibitor with IC50 of ~0.1 nM.
Last Update: 2026-04-17 13:46:08
CAS: 5142-23-4
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50mg, 100mg, 250mg, 500mg
Package: A145872
Price: 346, 504, 910, 1764 (in RMB)
Descriptions: 3-Methyladenine is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC50 of 25 μM and 60 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50mg, 100mg, 250mg, 500mg
Package: A145872
Price: 346, 504, 910, 1764 (in RMB)
Descriptions: 3-Methyladenine is a selective PI3K inhibitor for Vps34 and PI3Kγ with IC50 of 25 μM and 60 μM.
Last Update: 2026-04-17 13:46:08
CAS: 50-63-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg
Package: A233637
Price: 99, 200, 142, 218, 262, 315 (in RMB)
Descriptions: Chloroquine phosphate is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. It is an autophagy and toll-like receptor (TLR) inhibitor and is highly effective in controlling SARS-CoV-2 (COVID-19) infection in vitro (EC50 = 1.13 μM).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 10mg, 25mg, 50mg, 100mg
Package: A233637
Price: 99, 200, 142, 218, 262, 315 (in RMB)
Descriptions: Chloroquine phosphate is an antimalarial and anti-inflammatory agent widely used to treat malaria and rheumatoid arthritis. It is an autophagy and toll-like receptor (TLR) inhibitor and is highly effective in controlling SARS-CoV-2 (COVID-19) infection in vitro (EC50 = 1.13 μM).
Last Update: 2026-04-17 13:46:08
CAS: 54-05-7
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A136097
Price: 109, 385, 220, 315, 560, 1103 (in RMB)
Descriptions: Chloroquine is an antimalarial drug and also an autophagy inhibitor, with an IC50 value of 2.1 μM for inhibiting autophagy. Chloroquine has antimalarial, anti-inflammatory, and antitumor effects and can be used in research on autophagy and malaria treatment.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg
Package: A136097
Price: 109, 385, 220, 315, 560, 1103 (in RMB)
Descriptions: Chloroquine is an antimalarial drug and also an autophagy inhibitor, with an IC50 value of 2.1 μM for inhibiting autophagy. Chloroquine has antimalarial, anti-inflammatory, and antitumor effects and can be used in research on autophagy and malaria treatment.
Last Update: 2026-04-17 13:46:08
CAS: 154447-36-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A133122
Price: 119, 501, 409, 598, 1086, 1418, 1953, 5103 (in RMB)
Descriptions: LY294002 is a PI3K inhibitor with IC50 values of 0.5 μM for PI3Kα, 0.57 μM for PI3Kδ, and 0.97 μM for PI3Kβ. LY294002 has anti-tumor effects and is used to study the PI3K/AKT signaling pathway and related cancer treatments. LY294002 promotes the differentiation of mouse embryonic stem cells into insulin-producing cells and inhibits the fusion of myoblasts into myotubes.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A133122
Price: 119, 501, 409, 598, 1086, 1418, 1953, 5103 (in RMB)
Descriptions: LY294002 is a PI3K inhibitor with IC50 values of 0.5 μM for PI3Kα, 0.57 μM for PI3Kδ, and 0.97 μM for PI3Kβ. LY294002 has anti-tumor effects and is used to study the PI3K/AKT signaling pathway and related cancer treatments. LY294002 promotes the differentiation of mouse embryonic stem cells into insulin-producing cells and inhibits the fusion of myoblasts into myotubes.
Last Update: 2026-04-17 13:46:08
CAS: 571203-78-6
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A145112
Price: 315, 408, 960, 1488, 3630 (in RMB)
Descriptions: Erastin is a compound that interacts with VDAC, blocks and reverses mitochondrial depolarization after microtubule destabilizers in intact cells and antagonized tubulin-induced VDAC blockage in planar bilayers. It is also a ferroptosis inducer. (Unstable in solution, please prepare and use now).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 1mg, 2mg, 5mg, 10mg, 50mg
Package: A145112
Price: 315, 408, 960, 1488, 3630 (in RMB)
Descriptions: Erastin is a compound that interacts with VDAC, blocks and reverses mitochondrial depolarization after microtubule destabilizers in intact cells and antagonized tubulin-induced VDAC blockage in planar bilayers. It is also a ferroptosis inducer. (Unstable in solution, please prepare and use now).
Last Update: 2026-04-17 13:46:08
CAS: 88899-55-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg
Package: A614767
Price: 1089, 7250, 1764 (in RMB)
Descriptions: Bafilomycin A1 is an inhibitor of vacuolar H+-ATPase with IC50 of 0.44 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg
Package: A614767
Price: 1089, 7250, 1764 (in RMB)
Descriptions: Bafilomycin A1 is an inhibitor of vacuolar H+-ATPase with IC50 of 0.44 nM.
Last Update: 2026-04-17 13:46:08
CAS: 15663-27-1
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A210558
Price: 100, 116, 164, 232, 348, 918, 1543 (in RMB)
Descriptions: Cisplatin (CDDP) is an antitumor chemotherapeutic agent that induces DNA damage in cancer cells through DNA cross-linking. Cisplatin can activate ferroptosis and induce autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A210558
Price: 100, 116, 164, 232, 348, 918, 1543 (in RMB)
Descriptions: Cisplatin (CDDP) is an antitumor chemotherapeutic agent that induces DNA damage in cancer cells through DNA cross-linking. Cisplatin can activate ferroptosis and induce autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 866405-64-3
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A137399
Price: 119, 500, 163, 456, 665, 1358, 2170, 2930 (in RMB)
Descriptions: Dorsomorphin is a selective, ATP-competitive AMPK inhibitor (Ki of 109 nM in the absence of AMP) that selectively inhibits BMP type I receptors ALK2, ALK3, and ALK6, and reverses autophagy activation and anti-inflammatory effects induced by Urolithin A.Dorsomorphin promotes differentiation of human pluripotent stem cells into neural progenitor cells, promotes differentiation of both mouse and human pluripotent stem cells into cardiomyocytes, enhances adipogenic differentiation of human mesenchymal cells, and inhibits osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A137399
Price: 119, 500, 163, 456, 665, 1358, 2170, 2930 (in RMB)
Descriptions: Dorsomorphin is a selective, ATP-competitive AMPK inhibitor (Ki of 109 nM in the absence of AMP) that selectively inhibits BMP type I receptors ALK2, ALK3, and ALK6, and reverses autophagy activation and anti-inflammatory effects induced by Urolithin A.Dorsomorphin promotes differentiation of human pluripotent stem cells into neural progenitor cells, promotes differentiation of both mouse and human pluripotent stem cells into cardiomyocytes, enhances adipogenic differentiation of human mesenchymal cells, and inhibits osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 1219168-18-9
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A213616
Price: 139, 716, 203, 410, 598, 1380, 1960 (in RMB)
Descriptions: Dorsomorphin 2HCl is an AMPK inhibitor with an Ki value of 109 nM for AMPK. Dorsomorphin 2HCl inhibits the BMP signaling pathway and can be used in research on stem cell differentiation and bone regeneration.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A213616
Price: 139, 716, 203, 410, 598, 1380, 1960 (in RMB)
Descriptions: Dorsomorphin 2HCl is an AMPK inhibitor with an Ki value of 109 nM for AMPK. Dorsomorphin 2HCl inhibits the BMP signaling pathway and can be used in research on stem cell differentiation and bone regeneration.
Last Update: 2026-04-17 13:46:08
CAS: 161401-82-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A834991
Price: 359, 2375, 700, 2468, 4216 (in RMB)
Descriptions: Z-VAD-FMK (Z-VAD(OH)-FMK) is a pan caspase inhibitor. Z-VAD-FMK does not inhibit the activity of ubiquitin C-terminal hydrolase L1 (UCHL1) even at concentrations up to 440 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg
Package: A834991
Price: 359, 2375, 700, 2468, 4216 (in RMB)
Descriptions: Z-VAD-FMK (Z-VAD(OH)-FMK) is a pan caspase inhibitor. Z-VAD-FMK does not inhibit the activity of ubiquitin C-terminal hydrolase L1 (UCHL1) even at concentrations up to 440 μM.
Last Update: 2026-04-17 13:46:08
CAS: 16561-29-8
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A175370
Price: 239, 1519, 436, 1050, 1770, 3730 (in RMB)
Descriptions: Phorbol 12-myristate 13-acetate is a PKC-activating phorbol ester, increases the intracellular Ca2+ concentration ([Ca2+]i) in a dose-dependent manner, with an EC50 of 11.7 nM.Phorbol 12-myristate 13-acetate stimulates cardiac differentiation of mesenchymal stem cells and promotes hematopoietic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg
Package: A175370
Price: 239, 1519, 436, 1050, 1770, 3730 (in RMB)
Descriptions: Phorbol 12-myristate 13-acetate is a PKC-activating phorbol ester, increases the intracellular Ca2+ concentration ([Ca2+]i) in a dose-dependent manner, with an EC50 of 11.7 nM.Phorbol 12-myristate 13-acetate stimulates cardiac differentiation of mesenchymal stem cells and promotes hematopoietic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 25316-40-9
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg, 1g
Package: A130952
Price: 139, 792, 745, 1320, 2520, 3180, 4210 (in RMB)
Descriptions: Doxorubicin HCl is an effective inhibitor of DNA topoisomerase I and II, with IC50 values of 0.8 μM and 2.67 μM, respectively. Doxorubicin HCl has cytotoxic properties and induces apoptosis and autophagy, making it a widely used chemotherapeutic agent in cancer treatment.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 500mg, 1g
Package: A130952
Price: 139, 792, 745, 1320, 2520, 3180, 4210 (in RMB)
Descriptions: Doxorubicin HCl is an effective inhibitor of DNA topoisomerase I and II, with IC50 values of 0.8 μM and 2.67 μM, respectively. Doxorubicin HCl has cytotoxic properties and induces apoptosis and autophagy, making it a widely used chemotherapeutic agent in cancer treatment.
Last Update: 2026-04-17 13:46:08
CAS: 616-91-1
Category: Inhibitors|Agonists, Cell Culture
Spec: 500mg, 1g, 5g, 10g
Package: A233740
Price: 280, 330, 350, 420 (in RMB)
Descriptions: Acetylcysteine is an inhibitor of ROS and the production of TNF. It is a pharmaceutical drug and nutritional supplement used as mucolytic agent.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 500mg, 1g, 5g, 10g
Package: A233740
Price: 280, 330, 350, 420 (in RMB)
Descriptions: Acetylcysteine is an inhibitor of ROS and the production of TNF. It is a pharmaceutical drug and nutritional supplement used as mucolytic agent.
Last Update: 2026-04-17 13:46:08
CAS: 152121-47-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A248150
Price: 109, 288, 263, 420, 685, 980, 1470, 1980 (in RMB)
Descriptions: SB 203580 is a selective p38 MAPK inhibitor with IC50 values of 50 nM for SAPK2a/p38 and 500 nM for SAPK2b/p38β2, without inhibiting JNK activity. It can activate autophagy and mitophagy. SB203580 enhances cardiomyocyte differentiation from human embryonic stem cells but inhibits cardiomyocyte differentiation from mouse embryonic stem cells by suppressing early mesoderm formation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A248150
Price: 109, 288, 263, 420, 685, 980, 1470, 1980 (in RMB)
Descriptions: SB 203580 is a selective p38 MAPK inhibitor with IC50 values of 50 nM for SAPK2a/p38 and 500 nM for SAPK2b/p38β2, without inhibiting JNK activity. It can activate autophagy and mitophagy. SB203580 enhances cardiomyocyte differentiation from human embryonic stem cells but inhibits cardiomyocyte differentiation from mouse embryonic stem cells by suppressing early mesoderm formation.
Last Update: 2026-04-17 13:46:08
CAS: 869185-85-3
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 50mg, 100mg
Package: A593990
Price: 231, 420, 980, 1470 (in RMB)
Descriptions: SB-203580 HCl is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 5mg, 10mg, 50mg, 100mg
Package: A593990
Price: 231, 420, 980, 1470 (in RMB)
Descriptions: SB-203580 HCl is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM.
Last Update: 2026-04-17 13:46:08
CAS: 129-56-6
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 250mg, 500mg
Package: A155219
Price: 109, 424, 216, 347, 535, 787, 1465, 2929 (in RMB)
Descriptions: SP600125 is a selective JNK inhibitor with high affinity for JNK1, JNK2, and JNK3, with IC50 values of 40 nM, 50 nM, and 90 nM, respectively. SP600125 has anti-inflammatory and antitumor effects and can be used in research on diseases related to the JNK signaling pathway.SP600125 inhibits BMP9-induced osteogenic differentiation of cultured mouse mesenchymal stem cells (MSCs) and primary bone marrow stromal cells, promotes adipogenic differentiation of human MSCs, but inhibits their osteogenic differentiation. When added during early stages of neuronal culture, SP600125 causes cell death and suppresses neurogenesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 250mg, 500mg
Package: A155219
Price: 109, 424, 216, 347, 535, 787, 1465, 2929 (in RMB)
Descriptions: SP600125 is a selective JNK inhibitor with high affinity for JNK1, JNK2, and JNK3, with IC50 values of 40 nM, 50 nM, and 90 nM, respectively. SP600125 has anti-inflammatory and antitumor effects and can be used in research on diseases related to the JNK signaling pathway.SP600125 inhibits BMP9-induced osteogenic differentiation of cultured mouse mesenchymal stem cells (MSCs) and primary bone marrow stromal cells, promotes adipogenic differentiation of human MSCs, but inhibits their osteogenic differentiation. When added during early stages of neuronal culture, SP600125 causes cell death and suppresses neurogenesis.
Last Update: 2026-04-17 13:46:08
CAS: 846557-71-9
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A722849
Price: 119, 591, 189, 472, 819, 1512, 2419, 3874 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A722849
Price: 119, 591, 189, 472, 819, 1512, 2419, 3874 (in RMB)
Descriptions: ML385 is an Nrf2 inhibitor that suppresses Nrf2 transcriptional activity with an IC50 value of 1.9 μM. ML385 has antioxidant and antitumor effects and is used in research on cancer and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
CAS: 146986-50-7
Category: Inhibitors|Agonists, Cell Culture
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A112358
Price: 252, 599, 760, 1865, 2665, 4799 (in RMB)
Descriptions: Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II with Ki values of 220 nM and 300 nM, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A112358
Price: 252, 599, 760, 1865, 2665, 4799 (in RMB)
Descriptions: Y-27632 is an orally active, ATP-competitive inhibitor of ROCK-I and ROCK-II with Ki values of 220 nM and 300 nM, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 129830-38-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A101744
Price: 119, 539, 300, 700, 900, 1740, 3200, 5800, 7600, 10800 (in RMB)
Descriptions: Y-27632 dihydrochloride is an ATP-competitive ROCK inhibitor with oral bioactivity. Y-27632 dihydrochloride has anti-epileptic properties .
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A101744
Price: 119, 539, 300, 700, 900, 1740, 3200, 5800, 7600, 10800 (in RMB)
Descriptions: Y-27632 dihydrochloride is an ATP-competitive ROCK inhibitor with oral bioactivity. Y-27632 dihydrochloride has anti-epileptic properties .
Last Update: 2026-04-17 13:46:08
CAS: 243984-11-4
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A888245
Price: 149, 847, 346, 693, 1071, 2590, 3654, 6237 (in RMB)
Descriptions: TAK-242, a small-molecule-specific inhibitor of Toll-like receptor (TLR)4 signaling, inhibits the production of lipopolysaccharide-induced inflammatory mediators by binding to the intracellular domain of TLR4.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A888245
Price: 149, 847, 346, 693, 1071, 2590, 3654, 6237 (in RMB)
Descriptions: TAK-242, a small-molecule-specific inhibitor of Toll-like receptor (TLR)4 signaling, inhibits the production of lipopolysaccharide-induced inflammatory mediators by binding to the intracellular domain of TLR4.
Last Update: 2026-04-17 13:46:08
CAS: 4311-88-0
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A181851
Price: 119, 550, 281, 450, 945, 1254 (in RMB)
Descriptions: Necrostatin-1 is an inhibitor of RIP1 and can decrease TNF-α-induced necroptosis with EC50 of 490 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A181851
Price: 119, 550, 281, 450, 945, 1254 (in RMB)
Descriptions: Necrostatin-1 is an inhibitor of RIP1 and can decrease TNF-α-induced necroptosis with EC50 of 490 nM.
Last Update: 2026-04-17 13:46:08
CAS: 1219810-16-8
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg, 1g
Package: A108537
Price: 169, 1019, 399, 665, 1050, 1575, 2520, 3276, 4914, 7585 (in RMB)
Descriptions: RSL3 ((1S,3R)-RSL3) is an inhibitor of glutathione peroxidase 4 (GPX4), which reduces GPX4 expression and induces ferroptosis in head and neck cancer cells. In HN3 resistant cells, it increases the protein levels of p62 and Nrf2, leading to Keap1 inactivation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg, 1g
Package: A108537
Price: 169, 1019, 399, 665, 1050, 1575, 2520, 3276, 4914, 7585 (in RMB)
Descriptions: RSL3 ((1S,3R)-RSL3) is an inhibitor of glutathione peroxidase 4 (GPX4), which reduces GPX4 expression and induces ferroptosis in head and neck cancer cells. In HN3 resistant cells, it increases the protein levels of p62 and Nrf2, leading to Keap1 inactivation.
Last Update: 2026-04-17 13:46:08
CAS: 109511-58-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A807258
Price: 169, 1056, 840, 1344, 2419, 3626 (in RMB)
Descriptions: U0126 is a highly selective inhibitor of both MEK1 and MEK2, a type of MAPK/ERK kinase. U-0126, when used in combination with FGF, Activin A, and PKC inhibitors, supports maintenance of human pluripotent stem cells, inhibits self-renewal, and leads to differentiation without affecting proliferation or survival.U-0126 also inhibits glutamate-induced oxidative stress in mouse hippocampal HT22 cells and primary rat cortical cultures and shows neuroprotective effects in a gerbil ischemia model and in hypoxic cultures of mouse primary neurons.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg
Package: A807258
Price: 169, 1056, 840, 1344, 2419, 3626 (in RMB)
Descriptions: U0126 is a highly selective inhibitor of both MEK1 and MEK2, a type of MAPK/ERK kinase. U-0126, when used in combination with FGF, Activin A, and PKC inhibitors, supports maintenance of human pluripotent stem cells, inhibits self-renewal, and leads to differentiation without affecting proliferation or survival.U-0126 also inhibits glutamate-induced oxidative stress in mouse hippocampal HT22 cells and primary rat cortical cultures and shows neuroprotective effects in a gerbil ischemia model and in hypoxic cultures of mouse primary neurons.
Last Update: 2026-04-17 13:46:08
CAS: 1173097-76-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A132258
Price: 119, 595, 295, 473, 769, 1323, 2171, 3128 (in RMB)
Descriptions: U0126 (U0126-EtOH) is a potent, non-ATP competitive, and selective MEK1 and MEK2 inhibitor with IC50 values of 72 nM and 58 nM, respectively. It also inhibits autophagy and mitophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A132258
Price: 119, 595, 295, 473, 769, 1323, 2171, 3128 (in RMB)
Descriptions: U0126 (U0126-EtOH) is a potent, non-ATP competitive, and selective MEK1 and MEK2 inhibitor with IC50 values of 72 nM and 58 nM, respectively. It also inhibits autophagy and mitophagy.
Last Update: 2026-04-17 13:46:08
CAS: 1032350-13-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A145592
Price: 129, 629, 261, 595, 820, 1418, 2030, 2870, 5166 (in RMB)
Descriptions: MK-2206 2HCl is a selective AKT inhibitor with IC50 values of 8 nM, 12 nM, and 65 nM for AKT1, AKT2, and AKT3, respectively. MK-2206 2HCl exhibits antitumor effects and is used in research on cancers related to the PI3K/AKT signaling pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A145592
Price: 129, 629, 261, 595, 820, 1418, 2030, 2870, 5166 (in RMB)
Descriptions: MK-2206 2HCl is a selective AKT inhibitor with IC50 values of 8 nM, 12 nM, and 65 nM for AKT1, AKT2, and AKT3, respectively. MK-2206 2HCl exhibits antitumor effects and is used in research on cancers related to the PI3K/AKT signaling pathway.
Last Update: 2026-04-17 13:46:08
CAS: 19542-67-7
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A107077
Price: 109, 385, 315, 409, 1386, 1890 (in RMB)
Descriptions: BAY 11-7082 is an inhibitor of IκBα phosphorylation and NF-κB. It selectively and irreversibly inhibits TNF-α-induced phosphorylation of IκB-α, decreases NF-κB activity, and reduces the expression of adhesion molecules. Additionally, BAY 11-7082 inhibits ubiquitin-specific proteases USP7 and USP21 (IC50 = 0.19, 0.96 μM, respectively), gasdermin D (GSDMD) pore formation in liposomes, and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A107077
Price: 109, 385, 315, 409, 1386, 1890 (in RMB)
Descriptions: BAY 11-7082 is an inhibitor of IκBα phosphorylation and NF-κB. It selectively and irreversibly inhibits TNF-α-induced phosphorylation of IκB-α, decreases NF-κB activity, and reduces the expression of adhesion molecules. Additionally, BAY 11-7082 inhibits ubiquitin-specific proteases USP7 and USP21 (IC50 = 0.19, 0.96 μM, respectively), gasdermin D (GSDMD) pore formation in liposomes, and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells.
Last Update: 2026-04-17 13:46:08
CAS: 256373-96-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A110681
Price: 109, 462, 315, 378, 553, 1197, 2016, 2505, 5796, 8101 (in RMB)
Descriptions: MCC950 sodium (CRID3 sodium salt) is an effective and selective NLRP3 inhibitor with IC50 values of 7.5 nM in BMDMs and 8.1 nM in HMDMs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g
Package: A110681
Price: 109, 462, 315, 378, 553, 1197, 2016, 2505, 5796, 8101 (in RMB)
Descriptions: MCC950 sodium (CRID3 sodium salt) is an effective and selective NLRP3 inhibitor with IC50 values of 7.5 nM in BMDMs and 8.1 nM in HMDMs.
Last Update: 2026-04-17 13:46:08
CAS: 210826-40-7
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A448777
Price: 150, 420, 665, 1365, 2240, 2783, 7791 (in RMB)
Descriptions: MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM in BMDMs.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A448777
Price: 150, 420, 665, 1365, 2240, 2783, 7791 (in RMB)
Descriptions: MCC950 is a potent, selective, small-molecule inhibitor of NLRP3 with IC50 of 7.5 nM in BMDMs.
Last Update: 2026-04-17 13:46:08
CAS: 167869-21-8
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A282482
Price: 129, 685, 233, 472, 682, 1953, 2583 (in RMB)
Descriptions: PD98059 is a non-ATP-competitive MEK inhibitor with IC50 values of 2-7 μM for MEK1 and 50 μM for MEK2, inhibiting MAPK activation and TCDD binding.PD98059 prevents differentiation of mouse ES cells, enhances adipogenic differentiation of human mesenchymal stem cells, and inhibits their osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg
Package: A282482
Price: 129, 685, 233, 472, 682, 1953, 2583 (in RMB)
Descriptions: PD98059 is a non-ATP-competitive MEK inhibitor with IC50 values of 2-7 μM for MEK1 and 50 μM for MEK2, inhibiting MAPK activation and TCDD binding.PD98059 prevents differentiation of mouse ES cells, enhances adipogenic differentiation of human mesenchymal stem cells, and inhibits their osteogenic differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 58-58-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A547954
Price: 259, 384, 751, 1417, 2667 (in RMB)
Descriptions: Puromycin 2HCl is an aminonucleoside antibiotic that acts as a protein synthesis inhibitor in mammalian cell lines selectively expressing transfected with the pac gene (Streptomyces alboa), and its product, puromycin acetyltransferase, inactivates the drug by acetylation, inducing intracellular DNA fragmentation in thymocytes and HL-60 leukemia. (The recommended range for transfection of mammalian cells is 1-30 μg/ml.)
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A547954
Price: 259, 384, 751, 1417, 2667 (in RMB)
Descriptions: Puromycin 2HCl is an aminonucleoside antibiotic that acts as a protein synthesis inhibitor in mammalian cell lines selectively expressing transfected with the pac gene (Streptomyces alboa), and its product, puromycin acetyltransferase, inactivates the drug by acetylation, inducing intracellular DNA fragmentation in thymocytes and HL-60 leukemia. (The recommended range for transfection of mammalian cells is 1-30 μg/ml.)
Last Update: 2026-04-17 13:46:08
CAS: 33069-62-4
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A238238
Price: 109, 400, 205, 328, 567, 945, 2450, 3800 (in RMB)
Descriptions: Paclitaxel is a natural antitumor drug that stabilizes the polymerization of tubulin, causing mitotic arrest and inducing apoptosis, ultimately leading to cell death. Paclitaxel also induces autophagy. Paclitaxel inhibits the initiation and growth of neurites in vitro by promoting microtubule polymerization.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A238238
Price: 109, 400, 205, 328, 567, 945, 2450, 3800 (in RMB)
Descriptions: Paclitaxel is a natural antitumor drug that stabilizes the polymerization of tubulin, causing mitotic arrest and inducing apoptosis, ultimately leading to cell death. Paclitaxel also induces autophagy. Paclitaxel inhibits the initiation and growth of neurites in vitro by promoting microtubule polymerization.
Last Update: 2026-04-17 13:46:08
CAS: 763113-22-0
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A134565
Price: 109, 397, 225, 361, 616, 910, 1386, 2495, 3465, 5198 (in RMB)
Descriptions: Olaparib is a PARP inhibitor with high affinity for PARP1 and PARP2, with IC50 values of 5 nM and 1 nM, respectively. Olaparib has antitumor effects and can be used in research on BRCA mutation-associated cancers.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A134565
Price: 109, 397, 225, 361, 616, 910, 1386, 2495, 3465, 5198 (in RMB)
Descriptions: Olaparib is a PARP inhibitor with high affinity for PARP1 and PARP2, with IC50 values of 5 nM and 1 nM, respectively. Olaparib has antitumor effects and can be used in research on BRCA mutation-associated cancers.
Last Update: 2026-04-17 13:46:08
CAS: 154-17-6
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A104420
Price: 153, 210, 252, 315, 938, 1490 (in RMB)
Descriptions: 2-Deoxy-D-glucose is a glucose analog that inhibits glycolysis by targeting hexokinase.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A104420
Price: 153, 210, 252, 315, 938, 1490 (in RMB)
Descriptions: 2-Deoxy-D-glucose is a glucose analog that inhibits glycolysis by targeting hexokinase.
Last Update: 2026-04-17 13:46:08
CAS: 50-02-2
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A144976
Price: 109, 208, 110, 165, 245, 350, 586, 1432 (in RMB)
Descriptions: Dexamethasone results in decrease in transmonolayer paracellular permeability mainly to sucrose, fluorescein and dextrans of up to 20 KDa in an immortalised rat brain endothelial cell line (GPNT).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A144976
Price: 109, 208, 110, 165, 245, 350, 586, 1432 (in RMB)
Descriptions: Dexamethasone results in decrease in transmonolayer paracellular permeability mainly to sucrose, fluorescein and dextrans of up to 20 KDa in an immortalised rat brain endothelial cell line (GPNT).
Last Update: 2026-04-17 13:46:08
CAS: 305834-79-1
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A261312
Price: 109, 303, 170, 378, 598, 1750, 2450, 3711 (in RMB)
Descriptions: SC79 is a specific Akt agonist capable of crossing the blood-brain barrier. It activates cytosolic Akt and inhibits Akt membrane translocation by specifically binding to the PH domain of Akt.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A261312
Price: 109, 303, 170, 378, 598, 1750, 2450, 3711 (in RMB)
Descriptions: SC79 is a specific Akt agonist capable of crossing the blood-brain barrier. It activates cytosolic Akt and inhibits Akt membrane translocation by specifically binding to the PH domain of Akt.
Last Update: 2026-04-17 13:46:08
CAS: 51-21-8
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A370752
Price: 109, 350, 158, 228, 283, 529 (in RMB)
Descriptions: 5-Fluorouracil is a potent antitumor compound that inhibits thymidylate synthase, depleting the intracellular dTTP pool by interfering with pyrimidine synthesis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A370752
Price: 109, 350, 158, 228, 283, 529 (in RMB)
Descriptions: 5-Fluorouracil is a potent antitumor compound that inhibits thymidylate synthase, depleting the intracellular dTTP pool by interfering with pyrimidine synthesis.
Last Update: 2026-04-17 13:46:08
CAS: 1268524-70-4
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A529842
Price: 129, 655, 588, 770, 1360, 1575, 2520, 3600 (in RMB)
Descriptions: (+)-JQ-1 (JQ1) is a potent, specific, and reversible BET bromodomain inhibitor, with IC50s of 77 and 33 nM for the first and second bromodomains (BRD4(1/2)). It also activates autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A529842
Price: 129, 655, 588, 770, 1360, 1575, 2520, 3600 (in RMB)
Descriptions: (+)-JQ-1 (JQ1) is a potent, specific, and reversible BET bromodomain inhibitor, with IC50s of 77 and 33 nM for the first and second bromodomains (BRD4(1/2)). It also activates autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 301836-41-9
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172016
Price: 129, 616, 350, 560, 2366, 3549 (in RMB)
Descriptions: SB-431542 is a TGF-β receptor kinase inhibitor (TRKI) in SMAD signaling.SB431542, in combination with LDN193189 or Noggin, promotes the differentiation of human pluripotent stem cell-derived neural progenitor cells, enhances proliferation and sheet formation of endothelial cells derived from mouse ES cells, boosts the differentiation of mouse and human pluripotent stem cells into cardiomyocytes, inhibits self-renewal of human pluripotent stem cells (PSCs), and induces their differentiation.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A172016
Price: 129, 616, 350, 560, 2366, 3549 (in RMB)
Descriptions: SB-431542 is a TGF-β receptor kinase inhibitor (TRKI) in SMAD signaling.SB431542, in combination with LDN193189 or Noggin, promotes the differentiation of human pluripotent stem cell-derived neural progenitor cells, enhances proliferation and sheet formation of endothelial cells derived from mouse ES cells, boosts the differentiation of mouse and human pluripotent stem cells into cardiomyocytes, inhibits self-renewal of human pluripotent stem cells (PSCs), and induces their differentiation.
Last Update: 2026-04-17 13:46:08
CAS: 338967-87-6
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A252480
Price: 109, 350, 252, 405, 791, 1379, 1930 (in RMB)
Descriptions: Mdivi-1 selectively inhibits mitochondrial division DRP1 and mitochondrial division Dynamin I (Dnm1), the IC50 is about 1-10 µM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A252480
Price: 109, 350, 252, 405, 791, 1379, 1930 (in RMB)
Descriptions: Mdivi-1 selectively inhibits mitochondrial division DRP1 and mitochondrial division Dynamin I (Dnm1), the IC50 is about 1-10 µM.
Last Update: 2026-04-17 13:46:08
CAS: 49843-98-3
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A142021
Price: 109, 370, 302, 403, 693, 1197, 1730 (in RMB)
Descriptions: EX-527 is a potent and selective SIRT1 inhibitor with IC50 of 38 nM, exhibits > 200-fold selectivity against SIRT2 and SIRT3.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A142021
Price: 109, 370, 302, 403, 693, 1197, 1730 (in RMB)
Descriptions: EX-527 is a potent and selective SIRT1 inhibitor with IC50 of 38 nM, exhibits > 200-fold selectivity against SIRT2 and SIRT3.
Last Update: 2026-04-17 13:46:08
CAS: 1797989-42-4
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A219562
Price: 129, 616, 378, 504, 693, 1470, 1764, 3465 (in RMB)
Descriptions: Laduviglusib monohydrochloride is a selective GSK-3 inhibitor with high affinity for GSK-3α and GSK-3β, with IC50 values of 2.2 nM and 1.5 nM, respectively. Laduviglusib has neuroprotective and anticancer effects and can be used in research on Alzheimer's disease and cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A219562
Price: 129, 616, 378, 504, 693, 1470, 1764, 3465 (in RMB)
Descriptions: Laduviglusib monohydrochloride is a selective GSK-3 inhibitor with high affinity for GSK-3α and GSK-3β, with IC50 values of 2.2 nM and 1.5 nM, respectively. Laduviglusib has neuroprotective and anticancer effects and can be used in research on Alzheimer's disease and cancer.
Last Update: 2026-04-17 13:46:08
CAS: 252917-06-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A133052
Price: 139, 788, 243, 409, 693, 1134, 1921, 2822, 4082 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) is an effective, selective, and orally active GSK-3α/β inhibitor used as an auxiliary agent in cell therapy.CHIR99021 promotes the differentiation of human induced pluripotent stem cells (iPSCs) into insulin-producing cells and the differentiation of human ES and iPS cells into cardiomyocytes.When used in combination with SB431542 and human recombinant LIF, CHIR99021 supports the generation and maintenance of primitive neural stem cells from human ES cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A133052
Price: 139, 788, 243, 409, 693, 1134, 1921, 2822, 4082 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) is an effective, selective, and orally active GSK-3α/β inhibitor used as an auxiliary agent in cell therapy.CHIR99021 promotes the differentiation of human induced pluripotent stem cells (iPSCs) into insulin-producing cells and the differentiation of human ES and iPS cells into cardiomyocytes.When used in combination with SB431542 and human recombinant LIF, CHIR99021 supports the generation and maintenance of primitive neural stem cells from human ES cells.
Last Update: 2026-04-17 13:46:08
CAS: 1782235-14-6
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A962469
Price: 149, 850, 302, 410, 605, 983, 1816, 2906, 4069 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) trihydrochloride serves as a potent and selective inhibitor of GSK-3α/β, with IC50 values of 10 nM and 6.7 nM. It exhibits >500-fold selectivity for GSK-3 over CDC2, ERK2, and other protein kinases. Additionally, Laduviglusib trihydrochloride acts as a potent activator of the Wnt/β-catenin signaling pathway, enhances self-renewal in mouse and human embryonic stem cells, and induces autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A962469
Price: 149, 850, 302, 410, 605, 983, 1816, 2906, 4069 (in RMB)
Descriptions: Laduviglusib (CHIR-99021) trihydrochloride serves as a potent and selective inhibitor of GSK-3α/β, with IC50 values of 10 nM and 6.7 nM. It exhibits >500-fold selectivity for GSK-3 over CDC2, ERK2, and other protein kinases. Additionally, Laduviglusib trihydrochloride acts as a potent activator of the Wnt/β-catenin signaling pathway, enhances self-renewal in mouse and human embryonic stem cells, and induces autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 871700-17-3
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A188937
Price: 109, 270, 153, 245, 546, 875 (in RMB)
Descriptions: Trametinib (GSK1120212; JTP-74057) is an orally active MEK inhibitor that inhibits MEK1 and MEK2 with IC50 values of about 2 nM. Trametinib activates autophagy and induces apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A188937
Price: 109, 270, 153, 245, 546, 875 (in RMB)
Descriptions: Trametinib (GSK1120212; JTP-74057) is an orally active MEK inhibitor that inhibits MEK1 and MEK2 with IC50 values of about 2 nM. Trametinib activates autophagy and induces apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 1187431-43-1
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A286366
Price: 129, 660, 224, 350, 490, 700 (in RMB)
Descriptions: Trametinib (DMSO solvate) (GSK-1120212 (DMSO solvate); JTP-74057 (DMSO solvate)) is an orally active MEK inhibitor that inhibits MEK1 and MEK2 with IC50s of about 2 nM, activating autophagy and inducing apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Autophagy
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A286366
Price: 129, 660, 224, 350, 490, 700 (in RMB)
Descriptions: Trametinib (DMSO solvate) (GSK-1120212 (DMSO solvate); JTP-74057 (DMSO solvate)) is an orally active MEK inhibitor that inhibits MEK1 and MEK2 with IC50s of about 2 nM, activating autophagy and inducing apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 475207-59-1
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1g
Package: A117299
Price: 109, 350, 1248 (in RMB)
Descriptions: Sorafenib Tosylate (Bay 43-9006 Tosylate) is a potent, orally active Raf inhibitor with IC50 values of 6 nM for Raf-1 and 20 nM for B-Raf. Sorafenib Tosylate is a multikinase inhibitor with IC50 values of 90 nM, 15 nM, 20 nM, 57 nM, and 58 nM for VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit, respectively. Sorafenib Tosylate induces autophagy and apoptosis, has anti-tumor activity, and is a ferroptosis activator.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1g
Package: A117299
Price: 109, 350, 1248 (in RMB)
Descriptions: Sorafenib Tosylate (Bay 43-9006 Tosylate) is a potent, orally active Raf inhibitor with IC50 values of 6 nM for Raf-1 and 20 nM for B-Raf. Sorafenib Tosylate is a multikinase inhibitor with IC50 values of 90 nM, 15 nM, 20 nM, 57 nM, and 58 nM for VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit, respectively. Sorafenib Tosylate induces autophagy and apoptosis, has anti-tumor activity, and is a ferroptosis activator.
Last Update: 2026-04-17 13:46:08
CAS: 284461-73-0
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A316727
Price: 109, 350, 153, 198, 409, 525, 756, 1150 (in RMB)
Descriptions: Sorafenib is a multi-kinase inhibitor that inhibits Raf-1 and B-RAF (IC50s = 6 and 22 µM, respectively), as well as the receptor tyrosine kinases VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit (IC50s = 90, 15, 20, 57, and 58 nM, respectively).
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg, 500mg, 1g
Package: A316727
Price: 109, 350, 153, 198, 409, 525, 756, 1150 (in RMB)
Descriptions: Sorafenib is a multi-kinase inhibitor that inhibits Raf-1 and B-RAF (IC50s = 6 and 22 µM, respectively), as well as the receptor tyrosine kinases VEGFR2, VEGFR3, PDGFRβ, FLT3, and c-Kit (IC50s = 90, 15, 20, 57, and 58 nM, respectively).
Last Update: 2026-04-17 13:46:08
CAS: 19983-44-9
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A109795
Price: 109, 385, 197, 315, 504, 819, 1260 (in RMB)
Descriptions: Stattic emerges as a potent STAT3 inhibitor, effectively inhibiting STAT3 phosphorylation (at Y705 and S727). It further inhibits the binding of a high-affinity phosphopeptide for the SH2 domain of STAT3 and ameliorates renal dysfunction in Alport syndrome (AS) mice.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Stem Cells
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A109795
Price: 109, 385, 197, 315, 504, 819, 1260 (in RMB)
Descriptions: Stattic emerges as a potent STAT3 inhibitor, effectively inhibiting STAT3 phosphorylation (at Y705 and S727). It further inhibits the binding of a high-affinity phosphopeptide for the SH2 domain of STAT3 and ameliorates renal dysfunction in Alport syndrome (AS) mice.
Last Update: 2026-04-17 13:46:08
CAS: 122111-03-9
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 25mg, 100mg, 250mg, 1g
Package: A309564
Price: 119, 554, 128, 287, 454, 703, 1953 (in RMB)
Descriptions: Gemcitabine Hydrochloride (LY 188011 Hydrochloride) is a pyrimidine nucleoside analog antimetabolite and antineoplastic agent that inhibits DNA synthesis and repair, leading to autophagy and apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 25mg, 100mg, 250mg, 1g
Package: A309564
Price: 119, 554, 128, 287, 454, 703, 1953 (in RMB)
Descriptions: Gemcitabine Hydrochloride (LY 188011 Hydrochloride) is a pyrimidine nucleoside analog antimetabolite and antineoplastic agent that inhibits DNA synthesis and repair, leading to autophagy and apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 95058-81-4
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 1g, 5g
Package: A433642
Price: 119, 554, 378, 454, 724, 1953, 3717 (in RMB)
Descriptions: Gemcitabine (LY 188011) is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent that hinders DNA synthesis and repair, leading to both autophagy and apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 50mg, 100mg, 250mg, 1g, 5g
Package: A433642
Price: 119, 554, 378, 454, 724, 1953, 3717 (in RMB)
Descriptions: Gemcitabine (LY 188011) is a pyrimidine nucleoside analog antimetabolite and an antineoplastic agent that hinders DNA synthesis and repair, leading to both autophagy and apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 129497-78-5
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A138297
Price: 169, 908, 216, 624, 958, 2150, 3310, 4820 (in RMB)
Descriptions: Verteporfin is a YAP inhibitor, which effectively destroys the YAP-TEAD interaction and induces cell apoptosis. At the same time, as an autophagy inhibitor, it specifically blocks the early stage of autophagy by preventing the formation of autophagy. Verteporfin, as a photosensitizer, can generate reactive oxygen species under illumination, and its IC50 value is 0.6nM. Verteporfin has anti-tumor and anti-angiogenesis effects, and can be used for photodynamic therapy and age-related macular degeneration.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A138297
Price: 169, 908, 216, 624, 958, 2150, 3310, 4820 (in RMB)
Descriptions: Verteporfin is a YAP inhibitor, which effectively destroys the YAP-TEAD interaction and induces cell apoptosis. At the same time, as an autophagy inhibitor, it specifically blocks the early stage of autophagy by preventing the formation of autophagy. Verteporfin, as a photosensitizer, can generate reactive oxygen species under illumination, and its IC50 value is 0.6nM. Verteporfin has anti-tumor and anti-angiogenesis effects, and can be used for photodynamic therapy and age-related macular degeneration.
Last Update: 2026-04-17 13:46:08
CAS: 1092939-17-7
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A157761
Price: 109, 228, 126, 256, 385, 552, 1071, 1722, 3021 (in RMB)
Descriptions: Ruxolitinib phosphate (INCB018424 phosphate) is a powerful JAK1/2 inhibitor with IC50 values of 3.3 nM and 2.8 nM, respectively, demonstrating more than 130-fold selectivity over JAK3.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A157761
Price: 109, 228, 126, 256, 385, 552, 1071, 1722, 3021 (in RMB)
Descriptions: Ruxolitinib phosphate (INCB018424 phosphate) is a powerful JAK1/2 inhibitor with IC50 values of 3.3 nM and 2.8 nM, respectively, demonstrating more than 130-fold selectivity over JAK3.
Last Update: 2026-04-17 13:46:08
CAS: 941678-49-5
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A272323
Price: 119, 578, 408, 693, 1223, 1764, 2835 (in RMB)
Descriptions: Ruxolitinib (INCB18424) is a potent and selective JAK1/2 inhibitor with IC50 values of 3.3 nM and 2.8 nM in cell-free assays. It has a 130-fold selectivity for JAK1/2 over JAK3. Ruxolitinib induces autophagy and kills tumor cells through toxic mitophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A272323
Price: 119, 578, 408, 693, 1223, 1764, 2835 (in RMB)
Descriptions: Ruxolitinib (INCB18424) is a potent and selective JAK1/2 inhibitor with IC50 values of 3.3 nM and 2.8 nM in cell-free assays. It has a 130-fold selectivity for JAK1/2 over JAK3. Ruxolitinib induces autophagy and kills tumor cells through toxic mitophagy.
Last Update: 2026-04-17 13:46:08
CAS: 179324-69-7
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A385479
Price: 109, 393, 321, 416, 945, 1134, 1827 (in RMB)
Descriptions: Bortezomib is a reversible and selective proteasome inhibitor that effectively inhibits the 20S proteasome by targeting threonine residues (Ki = 0.6 nM). Bortezomib is mainly used in the treatment research of multiple myeloma and other hematologic cancers.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A385479
Price: 109, 393, 321, 416, 945, 1134, 1827 (in RMB)
Descriptions: Bortezomib is a reversible and selective proteasome inhibitor that effectively inhibits the 20S proteasome by targeting threonine residues (Ki = 0.6 nM). Bortezomib is mainly used in the treatment research of multiple myeloma and other hematologic cancers.
Last Update: 2026-04-17 13:46:08
CAS: 6823-69-4
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A213331
Price: 567, 759, 1386, 2565, 4170, 5005 (in RMB)
Descriptions: GW4869 2HCl is a cell permeable, selective and non-competitve inhibitor of N-SMase (neutral sphingomyelinase), which is important in the metabolism of sphingomyelin producing ceramide and phosphocholine and in cell signaling and regulation. GW4869 is an exosome inhibitor.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Metabolic Enzyme
Spec: 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A213331
Price: 567, 759, 1386, 2565, 4170, 5005 (in RMB)
Descriptions: GW4869 2HCl is a cell permeable, selective and non-competitve inhibitor of N-SMase (neutral sphingomyelinase), which is important in the metabolism of sphingomyelin producing ceramide and phosphocholine and in cell signaling and regulation. GW4869 is an exosome inhibitor.
Last Update: 2026-04-17 13:46:08
CAS: 571190-30-2
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A295334
Price: 109, 379, 385, 490, 516, 700, 875, 1000, 1190, 1540 (in RMB)
Descriptions: Palbociclib is a highly specific inhibitor of Cdk4 and Cdk6 with IC50s of 11 nM and16 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A295334
Price: 109, 379, 385, 490, 516, 700, 875, 1000, 1190, 1540 (in RMB)
Descriptions: Palbociclib is a highly specific inhibitor of Cdk4 and Cdk6 with IC50s of 11 nM and16 nM.
Last Update: 2026-04-17 13:46:08
CAS: 827022-32-2
Category: Inhibitors|Agonists, Cell Cycle
Spec: 5mg, 10mg, 50mg, 100mg
Package: A165771
Price: 332, 425, 800, 1000 (in RMB)
Descriptions: Palbociclib (PD 0332991) monohydrochloride is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively. Palbociclib monohydrochloride exhibits potent anti-proliferative activity and induces cell cycle arrest in cancer cells, which is valuable for research on HR-positive and HER2-negative breast cancer and hepatocellular carcinoma.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 5mg, 10mg, 50mg, 100mg
Package: A165771
Price: 332, 425, 800, 1000 (in RMB)
Descriptions: Palbociclib (PD 0332991) monohydrochloride is an orally active selective CDK4 and CDK6 inhibitor with IC50 values of 11 and 16 nM, respectively. Palbociclib monohydrochloride exhibits potent anti-proliferative activity and induces cell cycle arrest in cancer cells, which is valuable for research on HR-positive and HER2-negative breast cancer and hepatocellular carcinoma.
Last Update: 2026-04-17 13:46:08
CAS: 1236188-16-1
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg
Package: A192145
Price: 630, 1764, 2999 (in RMB)
Descriptions: 740 Y-P is cell-permeable peptide activator of PI3K.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 1mg, 5mg, 10mg
Package: A192145
Price: 630, 1764, 2999 (in RMB)
Descriptions: 740 Y-P is cell-permeable peptide activator of PI3K.
Last Update: 2026-04-17 13:46:08
CAS: 827022-33-3
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A280869
Price: 119, 532, 157, 346, 504, 850, 1021, 1474, 3742 (in RMB)
Descriptions: Palbociclib isethionate is a highly specific inhibitor of Cdk4 (IC50=11 nM) and Cdk6 (IC50=16 nM), having no activity against a panel of 36 additional protein kinases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg
Package: A280869
Price: 119, 532, 157, 346, 504, 850, 1021, 1474, 3742 (in RMB)
Descriptions: Palbociclib isethionate is a highly specific inhibitor of Cdk4 (IC50=11 nM) and Cdk6 (IC50=16 nM), having no activity against a panel of 36 additional protein kinases.
Last Update: 2026-04-17 13:46:08
CAS: 1716-12-7
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg
Package: A455726
Price: 99, 174, 238, 357, 643 (in RMB)
Descriptions: Sodium 4-phenylbutyrate (4-PBA sodium) is an inhibitor of HDAC and endoplasmic reticulum (ER) stress, utilized in cancer and infection research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 50mg, 100mg, 250mg
Package: A455726
Price: 99, 174, 238, 357, 643 (in RMB)
Descriptions: Sodium 4-phenylbutyrate (4-PBA sodium) is an inhibitor of HDAC and endoplasmic reticulum (ER) stress, utilized in cancer and infection research.
Last Update: 2026-04-17 13:46:08
CAS: 1821-12-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 500mg, 1g, 5g
Package: A148817
Price: 99, 176, 126, 218, 262, 315 (in RMB)
Descriptions: 4-Phenylbutanoic acid is an inhibitor of HDAC which can regulate gene transcription with anti-tumor and neuroprotective effects.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 100mg, 500mg, 1g, 5g
Package: A148817
Price: 99, 176, 126, 218, 262, 315 (in RMB)
Descriptions: 4-Phenylbutanoic acid is an inhibitor of HDAC which can regulate gene transcription with anti-tumor and neuroprotective effects.
Last Update: 2026-04-17 13:46:08
CAS: 1257044-40-8
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 50mg, 100mg, 250mg, 1g
Package: A156386
Price: 119, 561, 189, 378, 529, 680, 882, 1932, 3679 (in RMB)
Descriptions: Venetoclax (ABT-199; GDC-0199) is a highly effective, selective, and orally active Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax can induce autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 50mg, 100mg, 250mg, 1g
Package: A156386
Price: 119, 561, 189, 378, 529, 680, 882, 1932, 3679 (in RMB)
Descriptions: Venetoclax (ABT-199; GDC-0199) is a highly effective, selective, and orally active Bcl-2 inhibitor with a Ki of less than 0.01 nM. Venetoclax can induce autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 10540-29-1
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A210874
Price: 133, 242, 350, 483, 1925, 2450 (in RMB)
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 100mg, 250mg, 500mg, 1g, 5g, 10g
Package: A210874
Price: 133, 242, 350, 483, 1925, 2450 (in RMB)
Last Update: 2026-04-17 13:46:08
CAS: 1809249-37-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A598153
Price: 189, 1299, 420, 980, 1540, 2870, 3360, 5040 (in RMB)
Descriptions: Remdesivir is an nucleotide-analog antiviral prodrug. Remdesivir could inhibit SARS-CoV-2 3CLpro main protease.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A598153
Price: 189, 1299, 420, 980, 1540, 2870, 3360, 5040 (in RMB)
Descriptions: Remdesivir is an nucleotide-analog antiviral prodrug. Remdesivir could inhibit SARS-CoV-2 3CLpro main protease.
Last Update: 2026-04-17 13:46:08
CAS: 950455-15-9
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A120662
Price: 169, 984, 472, 693, 1134, 1890, 2268, 3276 (in RMB)
Descriptions: Liproxstatin-1 is a selective fatty acid oxidation enzyme inhibitor with high affinity for fatty acid oxidation enzymes, with an IC50 value of 22 nM. Liproxstatin-1 exhibits antioxidant and anti-inflammatory effects and can be used in research on fatty acid metabolism and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A120662
Price: 169, 984, 472, 693, 1134, 1890, 2268, 3276 (in RMB)
Descriptions: Liproxstatin-1 is a selective fatty acid oxidation enzyme inhibitor with high affinity for fatty acid oxidation enzymes, with an IC50 value of 22 nM. Liproxstatin-1 exhibits antioxidant and anti-inflammatory effects and can be used in research on fatty acid metabolism and oxidative stress-related diseases.
Last Update: 2026-04-17 13:46:08
CAS: 915087-33-1
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A270395
Price: 129, 693, 233, 408, 656, 1541, 1956, 3276 (in RMB)
Descriptions: Enzalutamide (MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. It also activates autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A270395
Price: 129, 693, 233, 408, 656, 1541, 1956, 3276 (in RMB)
Descriptions: Enzalutamide (MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. It also activates autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 905579-51-3
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A724332
Price: 149, 847, 283, 515, 693, 1102, 1995, 2835, 4410 (in RMB)
Descriptions: Pevonedistat (MLN4924) showcases potent and selective inhibition of NEDD8-activating enzyme (NAE), with an IC50 of 4.7 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Ubiquitin
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A724332
Price: 149, 847, 283, 515, 693, 1102, 1995, 2835, 4410 (in RMB)
Descriptions: Pevonedistat (MLN4924) showcases potent and selective inhibition of NEDD8-activating enzyme (NAE), with an IC50 of 4.7 nM.
Last Update: 2026-04-17 13:46:08
CAS: 4474-91-3
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A594780
Price: 423, 679, 1090, 1570, 2320 (in RMB)
Descriptions: Angiotensin II human is a peptide hormone that causes vasoconstriction and a subsequent increase in blood pressure.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A594780
Price: 423, 679, 1090, 1570, 2320 (in RMB)
Descriptions: Angiotensin II human is a peptide hormone that causes vasoconstriction and a subsequent increase in blood pressure.
Last Update: 2026-04-17 13:46:08
CAS: 28643-80-3
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A359670
Price: 613, 898, 1470, 2030, 2842 (in RMB)
Descriptions: Nigericin sodium salt is an antibiotic obtained from Streptomyces hygroscopicus, acting as an H+, K+, and Pb2+ ion carrier and as an NLRP3 agonist.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 5mg, 10mg, 25mg, 50mg, 100mg
Package: A359670
Price: 613, 898, 1470, 2030, 2842 (in RMB)
Descriptions: Nigericin sodium salt is an antibiotic obtained from Streptomyces hygroscopicus, acting as an H+, K+, and Pb2+ ion carrier and as an NLRP3 agonist.
Last Update: 2026-04-17 13:46:08
CAS: 68521-88-0
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A489583
Price: 188, 470, 750, 1375, 1900, 2800 (in RMB)
Descriptions: Angiotensin II human (Angiotensin II) acetate acts as a vasoconstrictor and a major bioactive peptide of the renin/angiotensin system. It plays a central role in regulating human blood pressure, primarily mediated by interactions between Angiotensin II and the G-protein-coupled receptors (GPCRs) Angiotensin II type 1 receptor (AT1R) and Angiotensin II type 2 receptor (AT2R). Angiotensin II human acetate stimulates sympathetic nervous stimulation, increases aldosterone biosynthesis and renal actions, induces growth of vascular smooth muscle cells, increases collagen type I and III synthesis in fibroblasts, leading to thickening of the vascular wall and myocardium, and fibrosis. It also induces apoptosis and capillary formation from endothelial cells via the LOX-1 dependent redox-sensitive pathway.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, GPCR|G Protein Pathway
Spec: 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A489583
Price: 188, 470, 750, 1375, 1900, 2800 (in RMB)
Descriptions: Angiotensin II human (Angiotensin II) acetate acts as a vasoconstrictor and a major bioactive peptide of the renin/angiotensin system. It plays a central role in regulating human blood pressure, primarily mediated by interactions between Angiotensin II and the G-protein-coupled receptors (GPCRs) Angiotensin II type 1 receptor (AT1R) and Angiotensin II type 2 receptor (AT2R). Angiotensin II human acetate stimulates sympathetic nervous stimulation, increases aldosterone biosynthesis and renal actions, induces growth of vascular smooth muscle cells, increases collagen type I and III synthesis in fibroblasts, leading to thickening of the vascular wall and myocardium, and fibrosis. It also induces apoptosis and capillary formation from endothelial cells via the LOX-1 dependent redox-sensitive pathway.
Last Update: 2026-04-17 13:46:08
CAS: 22978-25-2
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A180779
Price: 109, 459, 168, 376, 567, 882, 1147, 1462 (in RMB)
Descriptions: GW9662 is a PPARγ antagonist with high selectivity for PPARγ, with an IC50 value of 3.3 nM. GW9662 has antidiabetic and anti-inflammatory effects and can be used in research on metabolic diseases and inflammatory disorders.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A180779
Price: 109, 459, 168, 376, 567, 882, 1147, 1462 (in RMB)
Descriptions: GW9662 is a PPARγ antagonist with high selectivity for PPARγ, with an IC50 value of 3.3 nM. GW9662 has antidiabetic and anti-inflammatory effects and can be used in research on metabolic diseases and inflammatory disorders.
Last Update: 2026-04-17 13:46:08
CAS: 187389-52-2
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A354225
Price: 189, 1224, 409, 1071, 1701, 3097, 3717 (in RMB)
Descriptions: Z-VAD(OMe)-FMK is a cell-permeable, irreversible broad-spectrum caspase inhibitor, blocks all features of apoptosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Apoptosis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg
Package: A354225
Price: 189, 1224, 409, 1071, 1701, 3097, 3717 (in RMB)
Descriptions: Z-VAD(OMe)-FMK is a cell-permeable, irreversible broad-spectrum caspase inhibitor, blocks all features of apoptosis.
Last Update: 2026-04-17 13:46:08
CAS: 66575-29-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A226193
Price: 109, 462, 209, 378, 510, 945, 1512, 2474 (in RMB)
Descriptions: Forskolin is an adenylyl cyclase activator that increases intracellular cAMP levels and activates PXR and FXR, commonly used in cell physiology research and autophagy induction. It has an IC50 of 41 nM and an EC50 of 0.5 μM. Forskolin enhances neural differentiation of rat hippocampal neural progenitor cells.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 50mg, 100mg, 250mg
Package: A226193
Price: 109, 462, 209, 378, 510, 945, 1512, 2474 (in RMB)
Descriptions: Forskolin is an adenylyl cyclase activator that increases intracellular cAMP levels and activates PXR and FXR, commonly used in cell physiology research and autophagy induction. It has an IC50 of 41 nM and an EC50 of 0.5 μM. Forskolin enhances neural differentiation of rat hippocampal neural progenitor cells.
Last Update: 2026-04-17 13:46:08
CAS: 61825-94-3
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A100048
Price: 197, 385, 573, 1031, 1800, 3060 (in RMB)
Descriptions: Oxaliplatin inhibits DNA synthesis by conforming DNA adducts.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 5mg, 50mg, 100mg, 250mg, 500mg, 1g
Package: A100048
Price: 197, 385, 573, 1031, 1800, 3060 (in RMB)
Descriptions: Oxaliplatin inhibits DNA synthesis by conforming DNA adducts.
Last Update: 2026-04-17 13:46:08
CAS: 62996-74-1
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg
Package: A256460
Price: 179, 1171, 416, 500, 924, 1638, 2771, 4379 (in RMB)
Descriptions: Staurosporine is a prototypical potent ATP-competitive multikinase inhibitor with IC50 of 0.7, 7, 8.5, 6, 20 nM for PKC, PKA,PKG, p60v-src tyrosine protein kinase, CaM kinase II, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Anti-infection
Spec: 50μL, 1mL, 1mg, 2mg, 5mg, 10mg, 25mg, 50mg
Package: A256460
Price: 179, 1171, 416, 500, 924, 1638, 2771, 4379 (in RMB)
Descriptions: Staurosporine is a prototypical potent ATP-competitive multikinase inhibitor with IC50 of 0.7, 7, 8.5, 6, 20 nM for PKC, PKA,PKG, p60v-src tyrosine protein kinase, CaM kinase II, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 326914-06-1
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A165303
Price: 109, 350, 252, 441, 927, 1575, 2100, 3024 (in RMB)
Descriptions: MHY1485 is a potent, cell-permeable mTOR activator that targets the ATP domain of mTOR and inhibits autophagy by suppressing the fusion between autophagosomes and lysosomes.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A165303
Price: 109, 350, 252, 441, 927, 1575, 2100, 3024 (in RMB)
Descriptions: MHY1485 is a potent, cell-permeable mTOR activator that targets the ATP domain of mTOR and inhibits autophagy by suppressing the fusion between autophagosomes and lysosomes.
Last Update: 2026-04-17 13:46:08
CAS: 657-24-9
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A270611
Price: 109, 440, 153, 198, 318, 453, 656 (in RMB)
Descriptions: Metformin (1,1-Dimethylbiguanide) activates AMPK by inhibiting mitochondrial respiratory chain in the liver, enhancing insulin sensitivity. It can be used in type 2 diabetes research and crosses the blood-brain barrier, inducing autophagy.Metformin, through activation of the PKC-CBP pathway, promotes neurogenesis in vitro in mouse cortical progenitor cells and human forebrain neural progenitor cells, as well as in vivo in the adult mouse central nervous system.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg
Package: A270611
Price: 109, 440, 153, 198, 318, 453, 656 (in RMB)
Descriptions: Metformin (1,1-Dimethylbiguanide) activates AMPK by inhibiting mitochondrial respiratory chain in the liver, enhancing insulin sensitivity. It can be used in type 2 diabetes research and crosses the blood-brain barrier, inducing autophagy.Metformin, through activation of the PKC-CBP pathway, promotes neurogenesis in vitro in mouse cortical progenitor cells and human forebrain neural progenitor cells, as well as in vivo in the adult mouse central nervous system.
Last Update: 2026-04-17 13:46:08
CAS: 1115-70-4
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 250μL, 5mg, 10mg, 25mg
Package: A122997
Price: 119, 279, 197, 315, 504 (in RMB)
Descriptions: Metformin hydrochloride (1,1-Dimethylbiguanide hydrochloride) inhibits the mitochondrial respiratory chain in the liver, activating AMPK and enhancing insulin sensitivity, which is useful in type 2 diabetes research. It also triggers autophagy.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 50μL, 250μL, 5mg, 10mg, 25mg
Package: A122997
Price: 119, 279, 197, 315, 504 (in RMB)
Descriptions: Metformin hydrochloride (1,1-Dimethylbiguanide hydrochloride) inhibits the mitochondrial respiratory chain in the liver, activating AMPK and enhancing insulin sensitivity, which is useful in type 2 diabetes research. It also triggers autophagy.
Last Update: 2026-04-17 13:46:08
CAS: 184475-35-2
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A109874
Price: 109, 424, 346, 498, 882, 1764 (in RMB)
Descriptions: Gefitinib (ZD1839) acts as a potent, selective, and orally active inhibitor of EGFR tyrosine kinase.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 100mg, 250mg, 1g, 5g
Package: A109874
Price: 109, 424, 346, 498, 882, 1764 (in RMB)
Descriptions: Gefitinib (ZD1839) acts as a potent, selective, and orally active inhibitor of EGFR tyrosine kinase.
Last Update: 2026-04-17 13:46:08
CAS: 184475-55-6
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 25mg, 100mg, 500mg, 1g, 5g
Package: A199522
Price: 129, 605, 288, 440, 760, 1120, 2240 (in RMB)
Descriptions: Gefitinib HCl is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. It suppresses cancer cell proliferation, promotes apoptosis, and reduces angiogenesis by blocking the PI3K and MAPK signaling pathways. It is used for EGFR mutation-positive non-small cell lung cancer and has also demonstrated antitumor activity in studies on solid tumors such as breast cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 25mg, 100mg, 500mg, 1g, 5g
Package: A199522
Price: 129, 605, 288, 440, 760, 1120, 2240 (in RMB)
Descriptions: Gefitinib HCl is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor. It suppresses cancer cell proliferation, promotes apoptosis, and reduces angiogenesis by blocking the PI3K and MAPK signaling pathways. It is used for EGFR mutation-positive non-small cell lung cancer and has also demonstrated antitumor activity in studies on solid tumors such as breast cancer.
Last Update: 2026-04-17 13:46:08
CAS: 58880-19-6
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 2mg, 5mg, 10mg
Package: A725112
Price: 209, 1397, 960, 1856, 3008 (in RMB)
Descriptions: Trichostatin A is a selective and potent HDAC inhibitor with IC50 of ~1.8 nM and HDAC8 is the only known member of the HDAC-family that is not affected by TSA.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 2mg, 5mg, 10mg
Package: A725112
Price: 209, 1397, 960, 1856, 3008 (in RMB)
Descriptions: Trichostatin A is a selective and potent HDAC inhibitor with IC50 of ~1.8 nM and HDAC8 is the only known member of the HDAC-family that is not affected by TSA.
Last Update: 2026-04-17 13:46:08
CAS: 9041-93-4
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg
Package: A1339440
Price: 459, 3091, 638, 946, 2610 (in RMB)
Descriptions: Bleomycin Sulfate is a water-soluble alkaline glycopeptide antibiotic, which specifically acts on S phase of cell cycle by inhibiting thymine incorporation into DNA and destroying DNA structure. Bleomycin Sulfate can be used to screen resistance and establish an animal model to induce experimental pulmonary fibrosis.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Apoptosis|Death Detection
Spec: 50μL, 1mL, 5mg, 10mg, 50mg
Package: A1339440
Price: 459, 3091, 638, 946, 2610 (in RMB)
Descriptions: Bleomycin Sulfate is a water-soluble alkaline glycopeptide antibiotic, which specifically acts on S phase of cell cycle by inhibiting thymine incorporation into DNA and destroying DNA structure. Bleomycin Sulfate can be used to screen resistance and establish an animal model to induce experimental pulmonary fibrosis.
Last Update: 2026-04-17 13:46:08
CAS: 67763-87-5
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg, 50mg, 100mg
Package: A338112
Price: 672, 1070, 2690, 3930 (in RMB)
Descriptions: Bleomycin hydrochloride is a DNA-damaging agent that inhibits DNA synthesis and is an antitumor antibiotic. Bleomycin plays a major role in the pathogenesis of scleroderma, promoting the gene transcription and protein synthesis of extracellular matrix components such as type I collagen, type III collagen, and fibronectin from skin fibroblasts, and inhibiting the activity of extracellular matrix-degrading enzymes.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 5mg, 10mg, 50mg, 100mg
Package: A338112
Price: 672, 1070, 2690, 3930 (in RMB)
Descriptions: Bleomycin hydrochloride is a DNA-damaging agent that inhibits DNA synthesis and is an antitumor antibiotic. Bleomycin plays a major role in the pathogenesis of scleroderma, promoting the gene transcription and protein synthesis of extracellular matrix components such as type I collagen, type III collagen, and fibronectin from skin fibroblasts, and inhibiting the activity of extracellular matrix-degrading enzymes.
Last Update: 2026-04-17 13:46:08
CAS: 284028-89-3
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A180960
Price: 109, 350, 264, 352, 868, 1172, 1758, 2924 (in RMB)
Descriptions: XAV-939 is a Tankyrase inhibitor used as an auxiliary agent in cell therapy. XAV939 induces cardiomyogenesis of mesodermal progenitor cells derived from mouse embryonic stem cells. When used in combination with SMAD inhibitors LDN193189 and SB431542, it promotes forebrain induction in human pluripotent stem cell lines.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg
Package: A180960
Price: 109, 350, 264, 352, 868, 1172, 1758, 2924 (in RMB)
Descriptions: XAV-939 is a Tankyrase inhibitor used as an auxiliary agent in cell therapy. XAV939 induces cardiomyogenesis of mesodermal progenitor cells derived from mouse embryonic stem cells. When used in combination with SMAD inhibitors LDN193189 and SB431542, it promotes forebrain induction in human pluripotent stem cell lines.
Last Update: 2026-04-17 13:46:08
CAS: 85622-93-1
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A137834
Price: 80, 100, 154, 231, 341, 410, 498, 784, 945, 4724 (in RMB)
Descriptions: Temozolomide is a DNA-methylating agent and an alkylating cytostatic drug used in the treatment of some brain cancers, astrocytoma and glioblastoma multiforme.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, DNA Damage Response (DDR) Pathway
Spec: 50μL, 1mL, 5mg, 10mg, 25mg, 50mg, 100mg, 500mg, 1g, 5g
Package: A137834
Price: 80, 100, 154, 231, 341, 410, 498, 784, 945, 4724 (in RMB)
Descriptions: Temozolomide is a DNA-methylating agent and an alkylating cytostatic drug used in the treatment of some brain cancers, astrocytoma and glioblastoma multiforme.
Last Update: 2026-04-17 13:46:08
CAS: 59865-13-3
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A473793
Price: 109, 458, 197, 298, 410, 936, 980 (in RMB)
Descriptions: Cyclosporine A is an immunosuppressive agent, binds to the cyclophilin and then inhibits calcineurin with IC50 of 7 nM.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Immunology|Inflammation
Spec: 50μL, 1mL, 25mg, 50mg, 100mg, 250mg, 500mg
Package: A473793
Price: 109, 458, 197, 298, 410, 936, 980 (in RMB)
Descriptions: Cyclosporine A is an immunosuppressive agent, binds to the cyclophilin and then inhibits calcineurin with IC50 of 7 nM.
Last Update: 2026-04-17 13:46:08
CAS: 117-39-5
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5g, 25g, 100g
Package: A1453902
Price: 109, 400, 132, 176, 379 (in RMB)
Descriptions: Quercetin is a natural flavonoid compound that activates SIRT1 and inhibits PI3K with an IC50 of 2.4 – 5.4 μM. It induces apoptosis and protective autophagy, commonly used in cancer research.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 5g, 25g, 100g
Package: A1453902
Price: 109, 400, 132, 176, 379 (in RMB)
Descriptions: Quercetin is a natural flavonoid compound that activates SIRT1 and inhibits PI3K with an IC50 of 2.4 – 5.4 μM. It induces apoptosis and protective autophagy, commonly used in cancer research.
Last Update: 2026-04-17 13:46:08
CAS: 849061-97-8
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 5g
Package: A1257621
Price: 106 (in RMB)
Descriptions: Quercetin hydrate, a natural flavonoid, stimulates recombinant SIRT1 and inhibits PI3K with IC50 values of 2.4 μM, 3.0 μM, and 5.4 μM for PI3K γ, PI3K δ, and PI3K β, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, PI3K|AKT|mTOR Pathway
Spec: 5g
Package: A1257621
Price: 106 (in RMB)
Descriptions: Quercetin hydrate, a natural flavonoid, stimulates recombinant SIRT1 and inhibits PI3K with IC50 values of 2.4 μM, 3.0 μM, and 5.4 μM for PI3K γ, PI3K δ, and PI3K β, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 6151-25-3
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 250mg, 1g
Package: A114540
Price: 109, 308, 196, 504 (in RMB)
Descriptions: Quercetin dihydrate, a natural flavonoid, stimulates recombinant SIRT1 and inhibits PI3K with IC50 values of 2.4 μM, 3.0 μM, and 5.4 μM for PI3K γ, PI3K δ, and PI3K β, respectively.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Cycle
Spec: 50μL, 1mL, 250mg, 1g
Package: A114540
Price: 109, 308, 196, 504 (in RMB)
Descriptions: Quercetin dihydrate, a natural flavonoid, stimulates recombinant SIRT1 and inhibits PI3K with IC50 values of 2.4 μM, 3.0 μM, and 5.4 μM for PI3K γ, PI3K δ, and PI3K β, respectively.
Last Update: 2026-04-17 13:46:08
CAS: 1421373-66-1
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 1g
Package: A188322
Price: 109, 459, 155, 315, 441, 735, 882, 1197, 2205, 4851 (in RMB)
Descriptions: Osimertinib mesylate (AZD9291 mesylate) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. It overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Angiogenesis
Spec: 50μL, 1mL, 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 250mg, 1g
Package: A188322
Price: 109, 459, 155, 315, 441, 735, 882, 1197, 2205, 4851 (in RMB)
Descriptions: Osimertinib mesylate (AZD9291 mesylate) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. It overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
Last Update: 2026-04-17 13:46:08
CAS: 1421373-65-0
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A157172
Price: 109, 385, 315, 441, 882, 1197 (in RMB)
Descriptions: Osimertinib (AZD9291) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. It overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
Last Update: 2026-04-17 13:46:08
Category: Inhibitors|Agonists, Cell Culture
Spec: 50μL, 1mL, 5mg, 10mg, 50mg, 100mg
Package: A157172
Price: 109, 385, 315, 441, 882, 1197 (in RMB)
Descriptions: Osimertinib (AZD9291) is a covalent, orally active, irreversible, and mutant-selective EGFR inhibitor with an apparent IC50 of 12 nM against L858R and 1 nM against L858R/T790M. It overcomes T790M-mediated resistance to EGFR inhibitors in lung cancer.
Last Update: 2026-04-17 13:46:08