微管蛋白
天然产物
秋水仙碱
化学
药理学
计算生物学
微管
生物
生物化学
细胞生物学
遗传学
作者
Mengqi Dong,Fang Liu,Hongyu Zhou,Shumei Zhai,Bing Yan
出处
期刊:Molecules
[MDPI AG]
日期:2016-10-15
卷期号:21 (10): 1375-1375
被引量:70
标识
DOI:10.3390/molecules21101375
摘要
Tubulin inhibitors are effective anticancer agents, however, there are many limitations to the use of available tubulin inhibitors in the clinic, such as multidrug resistance, severe side-effects, and generally poor bioavailability. Thus, there is a constant need to search for novel tubulin inhibitors that can overcome these limitations. Natural product and privileged structures targeting tubulin have promoted the discovery and optimization of tubulin inhibitors. This review will focus on novel tubulin inhibitors derived from natural products and privileged structures targeting the colchicine binding site on tubulin.
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