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- 技术资料
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
10 mM * 1 mL/1 mg/2 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥1209.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥449.0 |
| 规格: | 2 mg | 产品价格: | ¥650.0 |
| 规格: | 5 mg | 产品价格: | ¥1200.0 |
| 规格: | 10 mg | 产品价格: | ¥1800.0 |
| 规格: | 25 mg | 产品价格: | ¥3188.0 |
| 规格: | 50 mg | 产品价格: | ¥4800.0 |
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Ipatasertib
CAS No. : 1001264-89-6
MCE 国际站:Ipatasertib
产品活性:Ipatasertib (GDC-0068) 是一种口服有效的、高选择性和 ATP 竞争性泛 Akt 抑制剂,其对 Akt1/2/3 的 IC50 值分别为 5、18、8 nM。Ipatasertib 通过抑制 Akt 导致非 p53 依赖性的 PUMA 激活,从而同步激活 FoxO3a 和 NF-κB 。Ipatasertib 还能诱导癌细胞凋亡 (apoptosis),抑制异种移植小鼠模型中的肿瘤生长。
研究领域:PI3K/Akt/mTOR | Apoptosis
In Vitro: Ipatasertib (10 µM; 12, 24 h) suppresses colon cancer cell proliferation by p53 irrespectively activating PUMA in vitro.
Ipatasertib (1, 5, 10, 20 μM; 24 h/10 μM; 3, 6, 12, 24 h) up-regulates the expression level of PUMA in a concentration and time dependent manner in HCT116 cells.
Ipatasertib increases the mRNA level of PUMA in HCT116 WT, p53−/−, and DLD1 (p53 mutant) cells.
Ipatasertib (10 µM; 24 h) induces apoptosis through PUMA/Bax pathway in HCT116 cells.
In Vivo: Ipatasertib (30 mg/kg; p.o.; single daily for 15 consecutive days) exhibits PUMA-dependent antitumor activity in HCT116 WT and PUMA−/− cells xenograft nude mice model.
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