| 常用名 | 1-[[(2S)-5-[(氨基亚胺甲基)氨基]-2-[[2-乙基-2-[(2-甲基-1-氧代丙基)氨基]-1-氧代丁基]氨基]-1-氧代戊基]氨基]-N-[二(4-氟苯基)甲基]环戊烷甲酰胺] | CAS号 | 1417329-24-8 |
|---|---|---|---|
| 价格 | 纯度 | 98.0% | |
| 备货期 | 10天 | 库存 | 现货 |
| 产品详情(用途,包装等)
用途: MM-102 is a potent WDR5/MLL interaction inhibitor, achieves IC50 = 2.4 nM with an estimated Ki 200 times more potent than the ARA peptide.IC50 value: 2.4 nMTarget: MLLin vitro: MM-102 inhibits MLL1 methyltransferase activity and MLL-1-induced HoxA9 and Meis-1 gene expression in leukemia cells expressing the MLL1-AF9 fusion gene. Also inhibits cell growth and induces apoptosis in leukemia cells harbouring MLL1 fusion proteins. MM-102, with the highest binding affinities to WDR5, also show the most potent inhibitory activity in the HMT assay with IC50 = 0.4-0.9 μM. MM-102 dose-dependently inhibits cell growth in the MV4;11 and KOPN8 leukemia cell lines, which carry MLL1-AF4 and MLL1-ENL fusion proteins, respectively. MM-102 has IC50 = 25 μM in both cell lines and completely inhibits cell growth in these cell lines at 75 μM. MM-102 effectively and selectively inhibits cell growth and induces apoptosis in leukemia cells harboring MLL1 fusion proteins and has minimal effect in leukemia cells with wild-type MLL1 protein.[1] 物理化学性质: CAS号:1417329-24-8 常用中文名:1-[[(2S)-5-[(氨基亚胺甲基)氨基]-2-[[2-乙基-2-[(2-甲基-1-氧代丙基)氨基]-1-氧代丁基]氨基]-1-氧代戊基]氨基]-N-[二(4-氟苯基)甲基]环戊烷甲酰胺] 常用英文名:MM-102 分子式:C35H49F2N7O4 分子量:669.80500 密度:N/A 沸点:N/A 熔点:N/A 闪点:N/A 储存条件:-20℃ |