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- 2025年12月05日
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- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
2541792-70-3
- 规格：
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥1603.0 |
|---|---|---|---|
| 规格： | 1 mg | 产品价格： | ￥1049.0 |
| 规格： | 5 mg | 产品价格： | ￥2000.0 |
| 规格： | 10 mg | 产品价格： | ￥3200.0 |
| 规格： | 25 mg | 产品价格： | ￥5760.0 |
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ASK1-IN-2
CAS No. : 2541792-70-3
MCE 国际站：ASK1-IN-2
产品活性：ASK1-IN-2 是一种有效的，具有口服活性的凋亡信号调节激酶 1 (ASK1) 抑制剂，IC50 值为 32.8 nM。ASK1-IN-2 可用于溃疡性结肠炎的研究。
研究领域：MAPK/ERK Pathway | Apoptosis
In Vitro: ASK1-IN-2 (compound 19) (10 mM; 1 h) inhibits the luciferase reporter activity in AP1-HEK293 cells, with inhibition rate of 95.59%.
In Vivo: ASK1-IN-2 (25 mg/kg; p.o. daily for 7 d) improves dextran sulphate sodium (DSS)-induced ulcerative colitis (UC) in mice.
ASK1-IN-2 (25 mg/kg; p.o. daily for 7 d) blocks ASK1-p38/JNK signaling pathways and reduces inflammatory cytokine levels in DSS-induced mouse colon tissues.
ASK1-IN-2 (1 mg/kg; i.v.) shows low clearance (CL=1.38 L/h/kg) and moderate half-life (T1/2=1.45 h) in rats.
ASK1-IN-2 (10 mg/kg; p.o.) shows high oral exposure (AUClast=4517 h•ng/mL), 62.2% oral bioavailability and acceptable terminal half-life (T1/2=2.31 h) in rats.
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文献和实验TRAF‐Mediated TNFR‐Family Signaling
chain. Cell 103:351‐361. Deng, Y., Ren, X., Yang, L., Lin, Y., and Wu, X. 2003. A JNK‐dependent pathway is required for TNFalpha‐induced apoptosis. Cell 115:61‐70
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