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Discovery of novel 2,4-diarylaminopyrimidine derivatives as potent and selective epidermal growth factor receptor (EGFR) inhibitors against L858R/T790M resistance mutation.

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第一作者: Qi,Yan
第一单位: School of Pharmacy, Fudan University, Shanghai, 201203, China.
作者: Qi,Yan [1] ; Yuzhe,Chen [2] ; Baiyou,Tang [3] ; Qiang,Xiao [1] ; Rong,Qu [2] ; Linjiang,Tong [4] ; Jian,Liu [1] ; Jian,Ding [4] ; Yi,Chen [4] ; Ning,Ding [1] ; Wenfu,Tan [5] ; Hua,Xie [6] ; Yingxia,Li [7]
作者单位: School of Pharmacy, Fudan University, Shanghai, 201203, China. [1] Division of Antitumor Pharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; University of Chinese Academy of Sciences, No.19A Yuquan Road, Beijing, 100049, China. [2] Division of Antitumor Pharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China; Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha, 410008, Hunan, China. [3] Division of Antitumor Pharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. [4] School of Pharmacy, Fudan University, Shanghai, 201203, China. Electronic address: wftan@fudan.edu.cn. [5] Division of Antitumor Pharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. Electronic address: hxie@simm.ac.cn. [6] School of Pharmacy, Fudan University, Shanghai, 201203, China. Electronic address: liyx417@fudan.edu.cn. [7]
DOI 10.1016/j.ejmech.2018.04.052
PMID 29730192
发布时间 2018-12-02
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European journal of medicinal chemistry

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