| 溶解性 | DMSO ≥93mg/mL Water <1.2mg/mL Ethanol ≥2.8mg/mL |
| 存贮条件 | 储存温度-20°C |
| 应用 | A potent inhibitor of EGFR T790M |
| 产品介绍 | WZ8040是突变选择型不可逆EGFRT790M抑制剂，对ERBB2磷酸化(T798I)无抑制性。 |
| 备注 | WZ8040 is a novel mutant-selective irreversible EGFRT790M inhibitor, does not inhibit ERBB2 phosphorylation (T798I). |
| 生化机理 | WZ8040 is 30- to 100-fold more potent against EGFR T790M, and up to 100-fold less potent against wild-type EGFR, than quinazoline-based EGFR inhibitors such as CL-387785 and HKI-272. WZ8040 treatment potently inhibits the growth of HCC827 (EGFR Del E746_A750), PC9 (EGFR Del E746_A750), H3255 (EGFR L858R), H1975 (EGFR L858R/T790M), and PC9 GR (EGFR Del E746_A750/T790M) with IC50 of 1 nM, 6 nM, 66 nM, 9 nM, and 8 nM, respectively. WZ8040 weakly inhibits the growth of HCC827 GR (EGFR E746_A750/MET amp), H1819 (ERBB2 amp), Calu-3 (ERBB2 amp), H1781 (ERBB2 Ins G776V, C), and HN11 (EGFR & ERBB2 WT) with IC50 of >3.3 μM, 738 nM, 915 nM, 744 nM, and 1.82 μM, respectively. WZ8040 is not toxic up to 10 μM against A549 (KRAS mutant) or H3122 (EML4-ALK) cells. |
| 别名 | WZ-8040; WZ 8040；N-[3-[[5-氯-2-[[4-(4-甲基-1-哌嗪基)苯基]氨基]-4-嘧啶基]硫基]苯基]-2-丙烯酰胺;WZ-8040;WZ 8040；N-[3-[[5-Chloro-2-[[4-(4-methyl-1-piperazinyl)phenyl]amino]-4-pyrimidinyl]thio]phenyl]-2-propenamide |
WZ8040
WZ8040 （订货以英文为准）
编号：W126471
CAS号：1214265-57-2
分子式：C24H25CLN6OS
分子量：481.02
| 产品名称 | WZ8040 |
| 中文名称 | WZ8040 |
| CAS号 | 1214265-57-2 |
| 分子式（M.F.） | C24H25CLN6OS |
| 分子量（M.W.） | 481.02 |
| 储存条件 | -20°C储存 |
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