Indole, a core nucleus for potent inhibitors of tubulin polymerization

被引:342
|
作者
Brancale, Andrea
Silvestri, Romano
机构
[1] Univ Roma La Sapienza, Ist Pasteur, Dipartimento Studi Farmaceut, Fdn Cenci Bolognetti, I-00185 Rome, Italy
[2] Cardiff Univ, Welsh Sch Pharm, Cardiff CF10 3XF, Wales
关键词
anti-tumor drugs; anti-mitotic agents; tubulin; indoles;
D O I
10.1002/med.20080
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Microtubules are the basic components of cell structure, which take part in a wide number of pivotal cellular functions. Drugs that are able to modulate the microtubule assembly either by inhibition of tubulin polymerization or by blocking microtubule disassembly are of great interest in anti-cancer therapy. Several tubulin polymerization inhibitors characterized by the presence of an indole nucleus have been obtained from natural sources or have been prepared by semi-synthesis. In the last decade an ever increasing number of synthetic indoles have been reported. We have reviewed anti-tubulin agents obtained by synthesis having an indole as core nucleus. The synthesis, the biological activity, and the structure-activity relationship aspects of 3-formyt-2-phenylindoles, heterocombretastatins, diarylindoles, 2-aroylindoles, D-24851, 2-aryl-3-aroylindoles, 3-aroyl- and 1-aroylindoles, and arylthioindoles are discussed. (c) 2006 Wiley Periodicals, Inc.
引用
收藏
页码:209 / 238
页数:30
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