细胞毒性
化学
抗生素
二氢叶酸还原酶
微生物学
结合
铁载体
小肠结肠炎耶尔森菌
药理学
细菌
生物
生物化学
体外
酶
数学分析
数学
基因
遗传学
作者
Sheng Zhao,Zhi‐Peng Wang,Zihua Lin,Guoxing Wei,Xumei Wen,Siyu Li,Xiaohong Yang,Qun Zhang,Chunmei Jing,Yuanwei Dai,Jian Guo,Yun He
标识
DOI:10.1002/anie.202204139
摘要
Drug repurposing is considered a promising strategy to fight antimicrobial resistance (AMR). Methotrexate (Mtx), a classical anticancer drug, could strongly inhibit bacterial dihydrofolate reductase (DHFR). However, its poor permeability into bacteria and potent human cytotoxicity make it unsuitable as an antibacterial. Herein, we reported the conjugation of Mtx with a siderophore to construct "Trojan horse" antibacterials. The most potent conjugate 8 with nanomolar minimum inhibitory concentration (MIC) values exhibited over 1.00×103 -fold improved activity against Gram-positive Streptococcus pneumoniae (S. pneumoniae) and Gram-negative Yersinia enterocolitica (Y. enterocolitica) compared with Mtx, while possessing 2.31×103 -fold reduced human cytotoxicity, resulting in 2.08×106 -fold improvements in the therapeutic index. This proof-of-principle study verifies that siderophore conjugation is an effective strategy for developing new antibacterials from anticancer drugs.
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