Tubulin-Interactive Natural Products as Anticancer Agents

被引:264
作者
Kingston, David G. I. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2009年 / 72卷 / 03期
关键词
CELL LUNG-CANCER; EVERY; 3; WEEKS; VASCULAR DISRUPTING AGENTS; DHA-PACLITAXEL TAXOPREXIN; II OPEN-LABEL; ANTINEOPLASTIC AGENTS; PHASE-II; BREAST-CANCER; HALICHONDRIN-B; ANTITUMOR AGENT;
D O I
10.1021/np800568j
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
This review provides an overview of the discovery, structures, and biological activities of anticancer natural products that act by inhibiting or promoting the assembly of tubulin to microtubules. The emphasis is on providing recent information on those compounds in clinical use or in advanced clinical trials. The vinca alkaloids, the combretastatins, NPI-2358, the halichondrin B analogue eribulin, dolastatin 10, noscapine, hemiasterlin, and rhizoxin are discussed as tubulin polymerization inhibitors, while the taxanes and the epothilones are the major classes of tubulin polymerization promoters presented, with brief treatments of discodermolide, eleutherobin, and laulimalide. The challenges and future directions of tubulin-interactive natural products-based drug discovery programs are also discussed briefly. © 2009 American Chemical Society and American Society of Pharmacognosy.
引用
收藏
页码:507 / 515
页数:9
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