| 溶解性 | DMSO 80 mg/mL Water 0.0001 mg/mL Ethanol <1 mg/mL |
| 存贮条件 | 储存温度-20°C |
| 备注 | MK-1775 is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM; hinders G2 DNA damage checkpoint. Phase 2. |
| 生化机理 | MK-1775 is a potent and selective Wee1 kinase inhibitor with an IC50 of 5.2 nM. |
| 别名 | 2-allyl-1-(6-(2-hydroxypropan-2-yl)pyridin-2-yl)-6-(4-(4-methylpiperazin-1-yl)phenylamino)-1,2-dihydropyrazolo[3,4-d]pyrimidin-3-one;2-allyl-1-(6-(2-hydroxypropan-2-yl)pyridin-2-yl)-6-(4-(4-methylpiperazin-1-yl)phenylamino)-1,2-dihydropyrazolo[3,4-d]pyrimidin-3-one |
MK-1775,Wee1激酶小分子抑制剂
MK-1775 （订货以英文为准）
编号：M127160
CAS号：955365-80-7
分子式：C27H32N8O2
分子量：500.61
| 产品名称 | MK-1775 |
| 中文名称 | MK-1775,Wee1激酶小分子抑制剂 |
| CAS号 | 955365-80-7 |
| 分子式（M.F.） | C27H32N8O2 |
| 分子量（M.W.） | 500.61 |
| 储存条件 | -20°C储存 |
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