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The human Aurora kinase inhibitor danusertib is a lead compound for anti-trypanosomal drug discovery via target repurposing

机译:人Aurora激酶抑制剂Danusertib是通过目标重新施加的抗锥体药物发现的铅化合物

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摘要

New drugs for neglected tropical diseases such as human African trypanosomiasis (HAT) are needed, yet drug discovery efforts are not often focused on this area due to cost. Target repurposing, achieved by the matching of essential parasite enzymes to those human enzymes that have been successfully inhibited by small molecule drugs, provides an attractive means by which new drug optimization programs can be pragmatically initiated. In this report we describe our results in repurposing an established class of human Aurora kinase inhibitors, typified by danusertib (>1), which we have observed to be an inhibitor of trypanosomal Aurora kinase 1 (TbAUK1) and effective in parasite killing in vitro. Informed by homology modeling and docking, a series of analogs of >1 were prepared that explored the scope of the chemotype and provided a nearly 25-fold improvement in cellular selectivity for parasite cells over human cells.
机译:需要用于被忽视的热带病的新药物,例如人类非洲锥虫病(HAT),但是由于成本的原因,药物发现工作并不经常集中在这一领域。通过将必需的寄生虫酶与已经被小分子药物成功抑制的人类酶相匹配而实现的目标重用,提供了一种有吸引力的方法,通过该方法可以务实地启动新的药物优化程序。在本报告中,我们描述了我们在重新使用已建立的以danusertib(> 1 )为代表的人类Aurora激酶抑制剂类别中的结果,我们发现该抑制剂是锥虫性Aurora激酶1(TbAUK1)的抑制剂,有效在体外杀死寄生虫。通过同源性建模和对接得知,制备了一系列> 1 的类似物,它们探索了化学型的范围,并提供了比人类细胞高25倍的寄生虫细胞选择性。

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