噻唑
金黄色葡萄球菌
抗菌活性
抗生素
药效团
化学
药品
抗生素耐药性
抗药性
药理学
抗菌剂
组合化学
微生物学
细菌
医学
生物
立体化学
生物化学
遗传学
作者
Jiaojiao Guo,Zhouling Xie,Wei Ruan,Qidong Tang,Dan Qiao,Wufu Zhu
标识
DOI:10.1016/j.ejmech.2023.115689
摘要
In recent years, the overuse of antibiotics has resulted in the emergence of antibiotic resistance, which is a serious global health problem. Methicillin-resistant Staphylococcus aureus (MRSA) is a common and virulent bacterium in clinical practice. Numerous researchers have focused on developing new candidate drugs that are effective, less toxic, and can overcome MRSA resistance. Thiazole derivatives have been found to exhibit antibacterial activity against drug-sensitive and drug-resistant pathogens. By hybridizing thiazole with other antibacterial pharmacophores, it is possible to obtain more effective antibacterial candidate drugs. Thiazole derivatives have shown potential in developing new drugs that can overcome drug resistance, reduce toxicity, and improve pharmacokinetic characteristics. This article reviews the recent progress of thiazole compounds as potential antibacterial compounds and examines the structure-activity relationship (SAR) in various directions. It covers articles published from 2018 to 2023, providing a comprehensive platform to plan and develop new thiazole-based small MRSA growth inhibitors with minimal side effects.
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