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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:
1080622-86-1
- 规格:
5 mg/10 mg/50 mg
| 规格: | 5 mg | 产品价格: | ¥800.0 |
|---|---|---|---|
| 规格: | 10 mg | 产品价格: | ¥1400.0 |
| 规格: | 50 mg | 产品价格: | ¥3800.0 |
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CP-466722
CAS No. : 1080622-86-1
MCE 国际站:CP-466722
产品活性:CP-466722 是一种可逆的 ATM 抑制剂,IC50 值为 0.41 μM,但对 PI3K,PIKK 家族蛋白没有作用。
研究领域:Cell Cycle/DNA Damage | PI3K/Akt/mTOR
作用靶点:ATM/ATR
In Vitro: CP-466722 (CP466722, 6-10 μM) inhibits IR-induced ATM kinase activity, and the inhibition can be rapidly and completely reversed. CP466722 (6, 10 μM) inhibits p53 induction and ATM-dependent phosphorylation in mouse cells, but CP466722 fails to inhibit ATR activity and ATR-dependent phosphorylation of Chk1. CP466722 (6 μM) disrupts ATM-dependent cell cycle checkpoints in cells. CP466722 (1 μM) completely inhibits ATM-dependent phosphorylation in MCF7 cells. CP466722 (10 μM) reduces pKAP1 phosphorylation in MCF7 cells, with an IC50 of 0.41 μM. CP466722 (10 μM) inhibits both pATM and pKAP1 signals. CP-466722 (CP466722, 5-50 μM) inhibits proliferation of SKBr-3 cancer cells more strongly than MCF-7 cancer cells. CP466722 (10 μM) also slightly increases proportions of MCF-7 and SKBr-3 cells in the G1 phase after treatment for 48 hours.
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