抗菌剂
金黄色葡萄球菌
耐甲氧西林金黄色葡萄球菌
抗生素
微生物学
抗生素耐药性
化学
细菌
生物
遗传学
作者
Jingjing Jia,Yan Luo,Xue Zhang,Ling He
标识
DOI:10.2174/0929867328666210322103340
摘要
Resistance to antibiotics has existed in the health care and community settings. Thus, developing novel antibiotics is urgent. Methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase (PK) is crucial for the survival of bacteria, making it a novel antimicrobial target. In the past decade, the most commonly reported PK inhibitors include indole, flavonoid, phenazine derivatives from natural products' small molecules or their analogs, or virtual screening from small molecule compound library. This review covers the PK inhibitors and their antimicrobial activities reported from the beginning of 2011 through mid-2020. The Structure-Activity Relationships (SARs) were discussed briefly as well.
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