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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:
CH5424802; RO5424802; RG7853
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- 规格:
1 mg/2 mg/5 mg/10 mg/50 mg/100 mg/200 mg
| 规格: | 1 mg | 产品价格: | ¥350.0 |
|---|---|---|---|
| 规格: | 2 mg | 产品价格: | ¥520.0 |
| 规格: | 5 mg | 产品价格: | ¥850.0 |
| 规格: | 10 mg | 产品价格: | ¥1050.0 |
| 规格: | 50 mg | 产品价格: | ¥2400.0 |
| 规格: | 100 mg | 产品价格: | ¥3850.0 |
| 规格: | 200 mg | 产品价格: | ¥5500.0 |
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Alectinib
CAS No. : 1256580-46-7
MCE 国际站:Alectinib
产品活性:Alectinib (CH5424802) 是一种有效、选择性、具有口服活性的 ALK 抑制剂,其 IC50 为 1.9 nM,Kd 值为 2.4 nM (以 ATP 竞争方式),并且还抑制 ALK F1174L 和 ALK R1275Q,其 IC50 分别为 1 nM 和 3.5 nM。Alectinib 还具有有效的中枢神经系统 (CNS) 渗透能力。
研究领域:Protein Tyrosine Kinase/RTK
作用靶点:Anaplastic lymphoma kinase (ALK)
In Vitro: Alectinib (0-1000 nM; 2 hours; NCI-H2228 cells) treatment could prevent autophosphorylation of ALK in NCI-H2228 cells expressing EML4-ALK, and it also resulted in substantial suppression of phosphorylation of STAT3 and AKT.
?Alectinib (0-1000 nM; 5 days; HCC827, A549, or NCIH522 cells) treatment reduces cell activity in a dose-dependent manner.
In Vivo: Alectinib (0.2-20 mg/kg; oral administration; once daily; for 11 days; SCID or nude mice bearing NCI-H2228 cells) treatment can result in dose-dependent tumor growth inhibition (EC50 of 0.46 mg/kg) and tumor regression. At any dose level, no differences in body weight or gross signs of toxicity are observed.
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