抗菌剂
化学
细菌
金黄色葡萄球菌
微生物学
抗生素耐药性
细胞毒性
细菌细胞结构
抗菌活性
革兰氏阳性菌
抗生素
生物化学
生物
体外
有机化学
遗传学
作者
Shuimu Lin,Liu JiaYong,Hongxia Li,Ying Liu,Yongzhi Chen,Jiachun Luo,Shouping Liu
标识
DOI:10.1021/acs.jmedchem.0c00433
摘要
The development of new antimicrobial agents capable of curing drug-resistant bacteria-induced infections is becoming a major challenge to the global healthcare system. To develop antimicrobials with new molecular entities, a series of novel carbazole-based compounds were designed and synthesized by biomimicking the structural properties and biological function of antimicrobial peptides. Compound 29 was selected as a lead compound from the structure–activity relationship analyses and biological activity evaluation. Compound 29 showed excellent antimicrobial activity against Gram-positive bacteria (MICs = 0.78–1.56 μg/mL), poor hemolytic activity (HC50 > 200 μg/mL), and low cytotoxicity to mammalian cells. Compound 29 had fast bactericidal properties and effectively prevented bacterial resistance in laboratory simulations. Antibacterial mechanism studies revealed that compound 29 directly destroyed bacterial cell membranes, leading to bacterial deaths. Importantly, compound 29 displayed an excellent efficacy in a murine bacterial keratitis model caused by Staphylococcus aureus ATCC29213.
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