Indole derivatives as tubulin polymerization inhibitors for the development of promising anticancer agents

被引:30
|
作者
Hong, Yu [1 ]
Zhu, Yuan-Yuan [1 ]
He, Qiuqin [2 ]
Gu, Shuang-Xi [3 ]
机构
[1] Wuhan Inst Technol, Sch Chem & Environm Engn, Wuhan 430205, Peoples R China
[2] Fudan Univ, Dept Chem, Shanghai 200433, Peoples R China
[3] Wuhan Inst Technol, Sch Chem Engn & Pharm, Minist Educ, Key Lab Green Chem Proc, Wuhan 430205, Peoples R China
基金
中国国家自然科学基金;
关键词
Anticancer; Indole derivatives; Microtubules; Tubulin polymerization inhibitors; Colchicine binding site; MICROWAVE-ASSISTED SYNTHESIS; BIOLOGICAL EVALUATION; IN-VITRO; ANTITUMOR-ACTIVITY; MOLECULAR DOCKING; TARGETING TUBULIN; BINDING-SITE; COMBRETASTATIN A-4; CYTOTOXIC ACTIVITY; STRUCTURAL BASIS;
D O I
10.1016/j.bmc.2021.116597
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The alpha-and beta-tubulins are the major polypeptide components of microtubules (MTs), which are attractive targets for anticancer drug development. Indole derivatives display a variety of biological activities including antitumor activity. In recent years, a great number of indole derivatives as tubulin polymerization inhibitors have sprung up, which encourages medicinal chemists to pursue promising inhibitors with improved antitumor activities, excellent physicochemical, pharmacokinetic and pharmacodynamic properties. In this review, the recent progress from 2010 to present in the development of indole derivatives as tubulin polymerization inhibitors was summarized and reviewed, which would provide useful clues and inspirations for further design of outstanding tubulin polymerization inhibitors.
引用
收藏
页数:21
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