尿素酶
毒力因子
伊布塞伦
幽门螺杆菌
化学
微生物学
酶
细菌
半胱氨酸
生物化学
尿素
变形杆菌
毒力
生物
谷胱甘肽
大肠杆菌
遗传学
谷胱甘肽过氧化物酶
基因
作者
Saurabh Loharch,Łukasz Berlicki
标识
DOI:10.1002/tcr.202200026
摘要
Urease, an enzyme that catalyzes the hydrolysis of urea, is a virulence factor of various pathogenic bacteria. In particular, Helicobacter pylori, that colonizes the digestive tract and Proteus spp., that can infect the urinary tract, are related to urease activity. Therefore, urease inhibitors are considered as potential therapeutics against these infections. This review describes current knowledge of the structures, activity, and biological importance of bacterial ureases. Moreover, the structure-based design of several classes of bacterial urease inhibitors is presented and discussed. Phosphinic and phosphonic acids were applied as transition-state analogues, while Michael acceptors and ebselen derivatives were applied as covalent binders of cysteine residue. This review incorporates bacterial urease inhibitors from literature published between 2008 and 2021.
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