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- 文献和实验
- 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:
1262041-49-5
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3190.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥1050.0 |
| 规格: | 5 mg | 产品价格: | ¥2900.0 |
| 规格: | 10 mg | 产品价格: | ¥4200.0 |
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GS-444217
CAS No. : 1262041-49-5
MCE 国际站:GS-444217
产品活性:GS-444217 是一种有效的,可口服的,选择性 ATP 竞争性凋亡信号调节激酶 1 (ASK1) 抑制剂,IC50 为 2.87 nM。
研究领域:MAPK/ERK Pathway | Apoptosis
In Vitro: Treatment with GS-444217 reduces ASK1 phosphorylation and prevents the phosphorylation of MKK3/6, MKK4, p38, and JNK at concentrations of 0.3 μM and above with full suppression of ASK1 activity at 1 μM. GS-444217 (1 μM) reduces ASK1 activity within 5 minutes of addition to the cultures, reaching a maximum level of inhibition by 30 minutes. Removal of GS-444217 from the cultures results in reactivation of ASK1 autophosphorylation within 10 minutes and near-complete recovery 2 hours after drug washout.
In Vivo: GS-444217 reduces oxidative stress (OS)-induced ASK1 signaling in kidney and inhibits acute renal tubular injury in rats. GS-444217 (30 mg/kg) inhibits activation of ASK1, p38, and JNK in rat kidney. GS-444217 has an in vivo EC50 of approximately 1.6 μM for inhibiting the ASK1 pathway in rodent kidney.
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文献和实验analysis and integration: of steps and arrows. Nat Genet, 22(3): 213-5. 17• Boguski MS. 1998. Data management and analysis for gene expression arrays. Nat. Genet., 20:1923. 18• Brazma A, Hingamp P, Quackenbush J, Sherlock G, Spellman P, Stoeckert C
New Gastroenterol,1996;2:3-5 [22] Huang PL,Zhu SN,Lu SL,Dai SZ,Jin YL.Inhibitor of fatty acid synthase induced apoptosis in human colonic cancer cells. World J Gastroentero,2000;6:295-297 [23] Sun ZX, Ma QW, Zhao TD, Wei YL, Wang GS, Li JS. Apoptosis
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