Discovery of N-((3R,4R)-4-Fluoro-1-(6-((3-methoxy-1-methyl-1H-pyrazol-4-yl)amino)-9-methyl-9H-purin-2-yl)pyrrolidine-3-yl)acrylamide (PF-06747775) through Structure-Based Drug Design: A High Affinity Irreversible Inhibitor Targeting Oncogenic EGFR Mutants with Selectivity over Wild-Type EGFR.
第一作者:
Simon,Planken
第一单位:
Wuxi AppTec, 288 Fute Zhong Road, Waigaoqiao Free Trade Zone, Shanghai 200131, China.
作者:
医学主题词
丙烯酰胺类(Acrylamides);动物(Animals);癌, 非小细胞肺(Carcinoma, Non-Small-Cell Lung);细胞系, 肿瘤(Cell Line, Tumor);狗(Dogs);药物设计(Drug Design);卤化作用(Halogenation);人类(Humans);肺(Lung);肺肿瘤(Lung Neoplasms);小鼠(Mice);模型, 分子(Models, Molecular);突变(Mutation);蛋白激酶抑制剂(Protein Kinase Inhibitors);吡咯烷类(Pyrrolidines);大鼠(Rats)
DOI
10.1021/acs.jmedchem.6b01894
PMID
28287730
发布时间
2018-12-22
- 浏览14
Journal of medicinal chemistry
3002-3019页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



