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杂环亲电试剂作为新型 MurA 抑制剂。

Heterocyclic electrophiles as new MurA inhibitors.

机构信息

Medicinal Chemistry Research Group, Research Centre for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.

Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.

出版信息

Arch Pharm (Weinheim). 2018 Dec;351(12):e1800184. doi: 10.1002/ardp.201800184. Epub 2018 Nov 21.

Abstract

An electrophilic fragment library of small heterocycles was developed and characterized in the surrogate GSH-reactivity assay and aqueous stability test that revealed their potential as covalent warheads. Screening the library against MurA from Staphylococcus aureus (MurA ) and Escherichia coli (MurA ) identified heterocyclic fragments with significant inhibitory potency. The validated heterocyclic warhead library might be useful for developing targeted covalent inhibitors for other targets of interest with a new design strategy incorporating heterocyclic electrophiles as warheads.

摘要

开发并表征了一个包含小杂环的亲电片段库,在替代 GSH 反应性测定和水稳定性测试中,这些杂环片段表现出作为共价弹头的潜力。对金黄色葡萄球菌(MurA)和大肠杆菌(MurA)的 MurA 进行文库筛选,发现具有显著抑制活性的杂环片段。验证后的杂环弹头文库可能对其他感兴趣靶点的靶向共价抑制剂的开发有用,新的设计策略将杂环亲电试剂作为弹头。

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