Recent advances of cytotoxic chalconoids targeting tubulin polymerization: Synthesis and biological activity

被引:82
|
作者
Mirzaei, Hassan [1 ]
Emami, Saeed [2 ,3 ]
机构
[1] Mazandaran Univ Med Sci, Pharmaceut Sci Res Ctr, Student Res Comm, Fac Pharm, Sari, Iran
[2] Mazandaran Univ Med Sci, Dept Med Chem, Fac Pharm, Sari, Iran
[3] Mazandaran Univ Med Sci, Pharmaceut Sci Res Ctr, Fac Pharm, Sari, Iran
关键词
Chalcones; 1,3-Diaryl-2-propen-1-ones; Anti-cancer; Cytotoxic activity; Tubulin polymerization; CELL-CYCLE ARREST; CHROMENE-BASED CHALCONES; ONE-POT SYNTHESIS; ANTICANCER AGENTS; ANTITUBULIN AGENTS; COMBRETASTATIN A-4; MILLEPACHINE DERIVATIVES; MEDICINAL CHEMISTRY; ANTIMITOTIC AGENTS; MOLECULAR DOCKING;
D O I
10.1016/j.ejmech.2016.05.067
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Since microtubules have an important role in mitosis and other vital cellular functions, tubulin-targeting chemotherapy has been received growing attention in anticancer drug design and development. It was found that a number of naturally occurring compounds including distinct chalcones exert their effect by inhibition of tubulin polymerization. After the identification of tubulin polymerization as potential target for chalcone-type compounds, extensive researches have been made to design and synthesis of new antitubulin chalconoids. Although diverse chalcones have found to be potent anticancer agents but in the present review, we focused on the recently reported tubulin polymerization inhibitors from chalcone origin and related synthetic compounds, and their detailed synthetic methods and biological activities. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:610 / 639
页数:30
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