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- 详细信息
- 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.
- 英文名:
AZD6738
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1352226-88-0
- 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: | ¥1089.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥586.0 |
| 规格: | 2 mg | 产品价格: | ¥800.0 |
| 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: | ¥3100.0 |
| 规格: | 50 mg | 产品价格: | ¥4500.0 |
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Ceralasertib
CAS No. : 1352226-88-0
MCE 国际站:Ceralasertib
产品活性:Ceralasertib (AZD6738) 是有效地 ATR 激酶抑制剂,IC50 值为 1 nM。
研究领域:Cell Cycle/DNA Damage | PI3K/Akt/mTOR
作用靶点:ATM/ATR
In Vitro: Ceralasertib (AZD6738) is a potent inhibitor of ATR kinase activity with an IC50 of 0.001 μM against the isolated enzyme and 0.074 μM against ATR kinase-dependent CHK1 phosphorylation in cells. Ceralasertib (AZD6738) induces cell death and senescence in non-small cell lung cancer (NSCLC) cell lines. Ceralasertib (AZD6738) impairs viability of four Kras mutant cell lines: H23, H460, A549, and H358. , with the lowest GI50 and greatest maximal inhibition in H460 and H23 cells (1.05 μM, 88.0% and 2.38 μM, 86.2%, respectively). Ceralasertib (AZD6738) potentiates the cytotoxicity of CDDP and NSC 613327 in NSCLC cell lines with intact ATM kinase signaling, and potently synergizes with CDDP in ATM-deficient NSCLC cells. Ceralasertib (AZD6738) inhibits human breast cancer cell lines with IC50 values less than 1 μM using MTT assay. Ceralasertib (AZD6738) induces cell cycle arrest and apoptosis. It downregulates DNA damage response molecules and cell proliferative signaling molecules.
In Vivo: Daily administration of Ceralasertib (AZD6738) and ATR kinase inhibition for 14 consecutive days is tolerated in mice and enhances the therapeutic efficacy of CDDP in xenograft models. Remarkably, the combination of CDDP and Ceralasertib (AZD6738) resolves ATM-deficient lung cancer xenografts.
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