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Toluidinesulfonamide hypoxia-induced factor 1 inhibitors: Alleviating drug-drug interactions through use of pubchem data and comparative molecular field analysis guided synthesis

机译:甲苯胺磺酰胺低氧诱导的因子1抑制剂:通过使用pubchem数据和比较分子场分析指导合成,减轻药物与药物的相互作用

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摘要

Inhibitors of hypoxia-inducible factor 1 (HIF-1) represent promising anticancer therapeutics. We have identified a series of potent toluidinesulfonamide HIF-1 inhibitors. However, the series was threatened by a potential liability to inhibit CYP2C9 which could cause dangerous drug-drug interactions when being coadministered with other drugs. We used structure-activity data from the PubChem database to develop a topomer CoMFAmodel that guided the design of novel sulfonamides with high selectivity for HIF-1 over CYP2C9 inhibition.
机译:缺氧诱导因子1(HIF-1)抑制剂代表了有希望的抗癌治疗药物。我们已经鉴定出一系列有效的甲苯胺磺酰胺HIF-1抑制剂。但是,该系列药物受到抑制CYP2C9的潜在责任的威胁,该CYP2C9与其他药物合用时可能引起危险的药物相互作用。我们使用来自PubChem数据库的结构活性数据开发了一种拓扑异构体CoMFA模型,该模型指导了对HIF-1的选择性高于对CYP2C9抑制作用的新型磺酰胺的设计。

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