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- 详细信息
- 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:
2098211-50-6
- 规格:
10 mM * 1 mL/1 mg/5 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥4290.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥2338.0 |
| 规格: | 5 mg | 产品价格: | ¥3900.0 |
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I-138
CAS No. : 2098211-50-6
MCE 国际站:I-138
产品活性:I-138 是一种口服有效的 USP1-UAF1 可逆抑制剂 (IC50: 4.1 nM; Ki: 5.4 nM),结构上与 ML323 (HY-17543) 相关。I-138 诱导细胞中 FANCD2 和 PCNA 的单泛素化,消除细胞中的 USP1 自裂解。
研究领域:Cell Cycle/DNA Damage
作用靶点:Deubiquitinase
In Vitro: I-138 (0.5 μM; 4 h) eliminates USP1 self-lysis in HAP-1 USP1 WT and knockout cells.
I-138 (0.5 μM; 4 h) induces the monoubiquitination of FANCD2 and PCNA in MDA-MB-436 cells.
(0.01-10 μM; 10 days) dose-dependently inhibits MDA-MB-436 cells viability and don't affect HCC1954 cells.
In Vivo: I-138 (50 mg/kg/day; po, for 41 days) results USP1 inhibition and modest antitumor activity in mice bearing MDA-MB-436 tumors. However, the combination of I-138 and Niraparib (HY-10619), a PARP inhibitor, benefit the BRCA1/2 mutant tumors inhibition in vivo.
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文献和实验1.103.90±0.95(1.20-5.00)138±2.90134_2.60(128-145)5.25±0.135.40±0.15(4.85-5.85)108±0.60107±0.55(105-110)26.2±2.1024.8±2.30(20.2-31.5)5.60±1.616.55±1.30(2.30-9.20)5.60±0.407.40±0.50(3.20-8.50)3.11±0.371.38±0.28(0.80-3.90)大鼠0.35±0.020.24±0.07(0.00-0.55)28
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