Elara Pharmaceuticals GmbH , Boxbergring 107, 69127 Heidelberg, Germany.
J Med Chem. 2011 Jun 9;54(11):3982-6. doi: 10.1021/jm200272h. Epub 2011 May 16.
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 CoMFA model that guided the design of novel sulfonamides with high selectivity for HIF-1 over CYP2C9 inhibition.
缺氧诱导因子 1(HIF-1)抑制剂是很有前途的抗癌治疗药物。我们已经鉴定出一系列有效的甲苯磺酰胺 HIF-1 抑制剂。然而,该系列受到抑制 CYP2C9 的潜在风险的威胁,当与其他药物同时使用时可能会导致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来开发拓扑 CoMFA 模型,该模型指导了新型磺胺类化合物的设计,这些磺胺类化合物对 HIF-1 的选择性高于 CYP2C9 的抑制。