Aristolactam A IIIa (Sch 546909) 是一种可以从 Glycosmis chlorosperma 中分离得到的马兜铃内酰胺型生物碱。Aristolactam A IIIa 是一种 DYRK1A 抑制剂。Aristolactam A IIIa 抑制花生四烯酸 (AA)、胶原蛋白和血小板活化因子 (PAF) 诱导的血小板聚集。Aristolactam A IIIa 对 HeLa 细胞具有较强的细胞毒性作用。
Amotosalen (S-59 (free base)) 是一种光活化的 DNA 和 RNA 交联的补骨脂素化合物，可用于中和病原体。光激活的 Amotosalen 可与 DNA 结合并使其永久交联，从而阻止 DNA 复制，进而抑制供体 T 细胞的增殖。Amotosalen 可用于研究血液系统病原体灭活技术和移植物抗宿主病 (GVHD)。
Dihydroflavokawin B 是一种选择性 COX-1 抑制剂，其 IC50 为 1.22 μM。Dihydroflavokawin B 可微弱抑制 COX-2 和 5-LOX。Dihydroflavokawin B 可抑制 Leishmania panamensis 和 Leishmania braziliensis 的前鞭毛体形式。Dihydroflavokawin B 可抑制由花生四烯酸、血小板活化因子和二磷酸腺苷诱导的兔血小板聚集。Dihydroflavokawin B 具有体外抗炎活性。Dihydroflavokawin B 可用于利什曼病的研究。
银杏内酯 B
Ginkgolide B (BN-52021) 是一种萜内酯，一种有效的血小板活化因子拮抗剂。Ginkgolide B 通过激活 PXR 保护内皮细胞免受外源性和内生性物质引起的损伤。Ginkgolide B 可透过脑血屏障。Ginkgolide B 具有抗氧化、抗炎、抗肿瘤和抗凋亡活性。Ginkgolide B 对缺血引起的损伤具有显着的神经保护作用。
银杏内酯 B (标准品)
Ginkgolide B (Standard)是 Ginkgolide B 的分析标准品。本产品用于研究及分析应用。Ginkgolide B (BN-52021) 是一种萜内酯，一种有效的血小板活化因子拮抗剂。Ginkgolide B 通过激活 PXR 保护内皮细胞免受外源性和内生性物质引起的损伤。Ginkgolide B 可透过脑血屏障。Ginkgolide B 具有抗氧化、抗炎、抗肿瘤和抗凋亡活性。Ginkgolide B 对缺血引起的损伤具有显着的神经保护作
Murrayafoline A 是一种可以从 Murraya tetramera 中提取的咔唑类生物碱。Murrayafoline A 直接靶向特异性蛋白 1 (Sp1)，从而抑制 NF-κB 和 MAPK 信号通路。Murrayafoline A 在血小板衍生生长因子 (PDGF) 刺激的血管平滑肌细胞中诱导 G0/G1 期阻滞。Murrayafoline A 通过促进细胞内 β-catenin 的降解减弱 Wnt/β-catenin 途径。Murrayafoline A 通过激活蛋白激酶 C 增强大鼠心室肌细胞的收缩和 L 型钙电流。Murrayafoline A 抑制体内 LPS (HY-D1056) 诱导的神经炎症。Murrayafoline A 可用于炎症、血管并发症和结肠癌研究。
Murrayafoline A (Standard) 是 Murrayafoline A (HY-W100287) 的分析标准品。本产品用于研究及分析应用。Murrayafoline A 是一种可以从 Murraya tetramera 中提取的咔唑类生物碱。Murrayafoline A 直接靶向特异性蛋白 1 (Sp1)，从而抑制 NF-κB 和 MAPK 信号通路。Murrayafoline A 在血小板衍生生长因子 (PDGF) 刺激的血管平
银杏内酯 B
Ginkgolide B (BN-52021) 是一种萜内酯，一种有效的血小板活化因子拮抗剂。Ginkgolide B 通过激活 PXR 保护内皮细胞免受外源性和内生性物质引起的损伤。Ginkgolide B 可透过脑血屏障。Ginkgolide B 具有抗氧化、抗炎、抗肿瘤和抗凋亡活性。Ginkgolide B 对缺血引起的损伤具有显着的神经保护作用。
Murrayafoline A 是一种可以从 Murraya tetramera 中提取的咔唑类生物碱。Murrayafoline A 直接靶向特异性蛋白 1 (Sp1)，从而抑制 NF-κB 和 MAPK 信号通路。Murrayafoline A 在血小板衍生生长因子 (PDGF) 刺激的血管平滑肌细胞中诱导 G0/G1 期阻滞。Murrayafoline A 通过促进细胞内 β-catenin 的降解减弱 Wnt/β-catenin 途径。Murrayafoline A 通过激活蛋白激酶 C 增强大鼠心室肌细胞的收缩和 L 型钙电流。Murrayafoline A 抑制体内 LPS (HY-D1056) 诱导的神经炎症。Murrayafoline A 可用于炎症、血管并发症和结肠癌研究。
银杏内酯 B (标准品)
Ginkgolide B (Standard)是 Ginkgolide B 的分析标准品。本产品用于研究及分析应用。Ginkgolide B (BN-52021) 是一种萜内酯，一种有效的血小板活化因子拮抗剂。Ginkgolide B 通过激活 PXR 保护内皮细胞免受外源性和内生性物质引起的损伤。Ginkgolide B 可透过脑血屏障。Ginkgolide B 具有抗氧化、抗炎、抗肿瘤和抗凋亡活性。Ginkgolide B 对缺血引起的损伤具有显着的神经保护作
Aristolactam A IIIa (Sch 546909) 是一种可以从 Glycosmis chlorosperma 中分离得到的马兜铃内酰胺型生物碱。Aristolactam A IIIa 是一种 DYRK1A 抑制剂。Aristolactam A IIIa 抑制花生四烯酸 (AA)、胶原蛋白和血小板活化因子 (PAF) 诱导的血小板聚集。Aristolactam A IIIa 对 HeLa 细胞具有较强的细胞毒性作用。
Murrayafoline A (Standard) 是 Murrayafoline A (HY-W100287) 的分析标准品。本产品用于研究及分析应用。Murrayafoline A 是一种可以从 Murraya tetramera 中提取的咔唑类生物碱。Murrayafoline A 直接靶向特异性蛋白 1 (Sp1)，从而抑制 NF-κB 和 MAPK 信号通路。Murrayafoline A 在血小板衍生生长因子 (PDGF) 刺激的血管平
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
MedchemExpress Validation 03
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
MedchemExpress Validation 04
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
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