1. Epigenetics Protein Tyrosine Kinase/RTK JAK/STAT Signaling Stem Cell/Wnt Immunology/Inflammation
  2. JAK Interleukin Related STAT
  3. JAK1-IN-20

JAK1-IN-20 (Compound 38) 是一种肠道限制性、口服活性的、选择性的 JAK1 抑制剂,IC50 为 <0.5 nM。JAK1-IN-20 可抑制 JAK1 的酶活性,并减少促炎细胞因子 (TNF-αIL-6) 的产生、抑制 STAT3 的磷酸化。JAK1-IN-20 可改善溃疡性结肠炎。JAK1-IN-20 可用于炎症性肠病的研究。

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JAK1-IN-20

JAK1-IN-20 Chemical Structure

CAS No. : 3106963-85-0

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

JAK1-IN-20 (Compound 38) is a gut-restricted, orally active, selective JAK1 inhibitor with an IC50 of <0.5 nM. JAK1-IN-20 inhibits the enzymatic activity of JAK1, reduces the production of proinflammatory cytokines (TNF-α, IL-6), and suppresses the phosphorylation of STAT3. JAK1-IN-20 ameliorates ulcerative colitis. JAK1-IN-20 can be used for the research of inflammatory bowel disease[1].

IC50 & Target[1]

JAK1

<0.5 nM (IC50)

IL-6

 

STAT3

 

体外研究
(In Vitro)

JAK1-IN-20 可强效且选择性地抑制 JAK1 酶活性,其 IC50 < 0.5 nM,对 JAK2、JAK3 和 TYK2 的选择性分别超过 312 倍、20000 倍和 354 倍[1]
JAK1-IN-20 (30 min) 可强效抑制 HEK-Blue IL-6 细胞中 IL-6 诱导的 JAK/STAT3 信号通路,其 IC50 为 28.0 nM[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: TF-1 cells, H9 cells
Concentration: Dose-response range; 100 nM, 500 nM (TF-1 cells, STAT3); 1000 nM (H9 cells, STAT1); 2000 nM (TF-1 cells, STAT5); 1000 nM tofacitinib (control)
Incubation Time: 1 h
Result: Potently suppressed IL-6-induced STAT3 phosphorylation with an IC50 of 218.6 nM.
Showed a concentration-dependent inhibitory profile and achieved comparable efficacy to 1000 nM tofacitinib at 100 nM.
Reduced IL-6-induced STAT3 phosphorylation at 500 nM.
Reduced IFN-α-induced STAT1 phosphorylation at 1000 nM.
Reduced GM-CSF-induced STAT5 phosphorylation at 2000 nM.
药代动力学
(Parmacokinetics)
Species Dose Route Plasma Concentration T1/2 AUC0-24 Vd CL Cmax Bioavailability
Rat[1] 1 mg/kg i.v. / 0.65 h 610 ng·h/mL 1.08 L/kg 27.5 mL/min/kg / /
Rat[1] 5 mg/kg p.o. / 1.3 h 254 ng·h/mL / / 167 ng/mL 8.3 %
Mice[1] 30 mg/kg p.o. <1 (0.5 h) ng/mL / / / / / /
体内研究
(In Vivo)

JAK1-IN-20 (10-30 mg/kg;灌胃;每日一次) 可显著改善 DSS 诱导的雌性 C57BL/6J 小鼠急性溃疡性结肠炎,降低疾病活动度、增加结肠长度、抑制促炎细胞因子的产生并改善结肠组织病理学表现[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6J (female, 7-8 weeks old, DSS-induced ulcerative colitis)[1]
Dosage: 10 mg/kg; 30 mg/kg
Administration: p.o.; daily
Result: Significantly reduced DAI scores compared to vehicle controls at 30 mg/kg.
Increased colon length and reduced colon wet weight relative to vehicle controls at 30 mg/kg.
Suppressed colon tissue TNF-α and IL-6 levels compared to vehicle controls at 30 mg/kg.
Reduced colonic tissue damage, including mucosal erosion, crypt architecture loss, and inflammatory cell infiltration, relative to vehicle controls at 30 mg/kg.
Demonstrated a dose-dependent improvement in disease outcomes.
分子量

537.97

Formula

C26H25ClFN7O3

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
JAK1-IN-20
目录号:
HY-181872
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