| 常用名 | HMS-101 | CAS号 | 1070690-06-0 |
|---|---|---|---|
| 价格 | ¥需询单/100mg ¥需询单/250mg ¥需询单/1g | 纯度 | 98.0% |
| 备货期 | 10天 | 库存 | 现货 |
| 产品详情(用途,包装等)
用途: HMS-101 (HMS101) is a potent, selective mutant IDH1 inhibitor, the IC50 is significantly lower in mouse bone marrow cells transduced with IDH1mut compared with IDH1wt (1 uM vs 12 uM, respectively); binds to the isocitrate-binding pocket of mutant IDH1, significantly reduces intracellular R-2HG levels in vitro HoxA9+IDH1mut cells at 10 uM; induces apoptosis in IDH1mut cells, markedly reduces phospho-ERK1/2 and the ratio of phospho-ERK/total-ERK, inhibits human AML cell growth. 物理化学性质: CAS号:1070690-06-0 常用中文名:HMS-101 常用英文名:HMS-101 分子式:C18H28FN3 分子量:305.433 密度:1.1±0.1 g/cm3 沸点:395.2±42.0 °C at 760 mmHg 熔点:N/A 闪点:192.8±27.9 °C |