吲哚试验
微管蛋白
部分
化学
解聚
立体化学
组合化学
药物发现
微管
计算生物学
生物化学
生物
有机化学
细胞生物学
作者
Fatima Naaz,Kumari Neha,Rafi Haider,Syed Shafi
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2021-10-01
卷期号:13 (20): 1795-1828
被引量:15
标识
DOI:10.4155/fmc-2020-0385
摘要
Tubulin inhibitors are conjugates that interfere with the dynamic equilibrium of the polymerization and depolymerization of microtubules. Among all the reported conjugates, indole moiety is one of the most significant classes for the development of new drug candidates for cancer therapy. Due to their presence in a wide range of natural as well as synthetic antitubulin agents, indole has become a versatile scaffold in research, and various synthetic and semisynthetic indole-based antitubulin agents have been identified and reported. The present article focuses on the reported indole-based tubulin inhibitors of synthetic origin from last the decade. Synthesis, structure-activity relationships and biological activities of synthetic indole derivatives along with brief updates on their antitubulin activity are presented.
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