排序酶A
金黄色葡萄球菌
化学
拟肽
化学空间
抗生素
细菌
生物膜
分拣酶
药物发现
微生物学
毒力
生物
生物化学
基因
肽
遗传学
作者
Rachit Sapra,Amit Kumar Rajora,T Vijaya Kumar,Govind P. Maurya,Nalin Pant,V. Haridas
标识
DOI:10.1021/acs.jmedchem.1c00386
摘要
Staphylococcus aureus is the leading cause of hospital-acquired infections. The enzyme sortase A, present on the cell surface of S. aureus, plays a key role in bacterial virulence without affecting the bacterial viability. Inhibition of sortase A activity offers a powerful but clinically less explored therapeutic strategy, as it offers the possibility of not inducing any selective pressure on the bacteria to evolve drug-resistant strains. In this Perspective, we offer a chemical space narrative for the design of sortase A inhibitors, as delineated into three broad domains: peptidomimetics, natural products, and synthetic small molecules. This provides immense opportunities for medicinal chemists to alleviate the ever-growing crisis of antibiotic resistance.
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