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Novel Natural Product- and Privileged Scaffold-Based Tubulin Inhibitors Targeting the Colchicine Binding Site

机译:靶向秋水仙碱结合位点的新型天然产物和特权支架的微管蛋白抑制剂。

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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.
机译:微管蛋白抑制剂是有效的抗癌药,但是,临床上对可用的微管蛋白抑制剂的使用存在许多局限性,例如多药耐药性,严重的副作用以及通常较差的生物利用度。因此,始终需要寻找可以克服这些局限性的新型微管蛋白抑制剂。靶向微管蛋白的天然产物和特权结构促进了微管蛋白抑制剂的发现和优化。这篇综述将集中在从天然产物和针对微管蛋白上秋水仙碱结合位点的特权结构衍生的新型微管蛋白抑制剂上。

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