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MycA 生物激活硫代烷基苯并恶唑前药家族对. 有效。

MymA Bioactivated Thioalkylbenzoxazole Prodrug Family Active against .

机构信息

Diseases of the Developing World (DDW), Global Health Catalyst, GlaxoSmithKline, Severo Ochoa 2, 28760 Tres Cantos, Madrid, Spain.

出版信息

J Med Chem. 2020 May 14;63(9):4732-4748. doi: 10.1021/acs.jmedchem.0c00003. Epub 2020 Apr 19.

Abstract

Screening of a GSK-proprietary library against intracellular identified , a thioalkylbenzoxazole hit. Biological profiling and mutant analysis revealed that this compound is a prodrug that is bioactivated by the mycobacterial enzyme MymA. A hit-expansion program including design, synthesis, and profiling of a defined set of analogues with optimized drug-like properties led to the identification of an emerging lead compound, displaying potency against intracellular bacteria in the low micromolar range, high in vitro solubility and permeability, and excellent microsomal stability.

摘要

筛选 GSK 专有文库以鉴定一种硫代烷氧基苯并恶唑命中靶标。生物特征分析和突变分析显示,该化合物是一种前药,可被分枝杆菌酶 MymA 生物激活。命中扩展计划包括设计、合成和对一组具有优化药物特性的已知类似物进行分析,最终确定了一种新兴的先导化合物,对细胞内细菌具有低微摩尔范围的效力、高体外溶解度和通透性,以及优异的微粒体稳定性。

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