Discovery of novel pyrrolo[2,3-b]pyridine derivatives bearing 1,2,3-triazole moiety as c-Met kinase inhibitors

被引:44
|
作者
Tang, Qidong [1 ,3 ]
Wang, Linxiao [1 ]
Tu, Yayi [1 ]
Zhu, Wufu [1 ]
Luo, Rong [2 ]
Tu, Qidong [1 ]
Wang, Ping [1 ]
Wu, Chunjiang [1 ]
Gong, Ping [3 ]
Zheng, Pengwu [1 ]
机构
[1] Jiangxi Sci & Technol Normal Univ, Sch Pharm, Nanchang 330013, Peoples R China
[2] Jiangxi Prov Inst Mat Med, Nanchang 330000, Peoples R China
[3] Shenyang Pharmaceut Univ, Sch Pharmaceut Engn, Key Lab Struct Based Drug Design & Discovery, Minist Educ, Shenyang 110016, Peoples R China
关键词
Synthesis; Pyrrolo[2,3-b]pyridine derivatives; 1,2,3-Triazole; c-Met; Antiproliferative activity; PROSTATE-CANCER; DESIGN; IDENTIFICATION; GROWTH;
D O I
10.1016/j.bmcl.2016.02.059
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of novel pyrrolo[2,3-b]pyridine derivatives bearing 1,2,3-triazole moiety were designed, synthesized, and evaluated for their c-Met kinase inhibitory activities and antiproliferative activities against 4 cancer cell lines (HT-29, A549, MCF-7, and PC-3) in vitro. Most compounds showed moderate to excellent potency, with the most promising analog 34 showing a c-Met IC50 value of 1.68 nM. Structure-activity relationship studies indicated that electron-withdrawing groups (X = CF3, R-1 = F, R-2 = 4-F) were required to decrease the higher electron density on the 5-atom linker to a proper degree to improve the inhibitory activity. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1680 / 1684
页数:5
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