体内
化学
抗菌剂
抗生素
运输机
生物化学
屎肠球菌
跨膜蛋白
计算生物学
微生物学
生物活性
大肠杆菌
表型筛选
蜡螟
体外
细菌
毒力因子
达尼奥
秀丽隐杆线虫
细胞
肠球菌
抗菌剂
染色体易位
药物发现
酶
粪肠球菌
模式生物
脂质Ⅱ
对接(动物)
作者
Ioulia Exapicheidou,Aleksei Tsarenko,Lena Zeller,Hamza Ibrahim,Carole Baumann,Atanaz Shams,Patrick A. Hoffmann,Yue Li,Andreas M. Kany,Jennifer Hermann,Dirk J. Slotboom,Rolf Müller,Andrea Volkamer,Mostafa M. Hamed,Eleonora Diamanti,Anna K. H. Hirsch
标识
DOI:10.1021/acs.jmedchem.5c02721
摘要
High Resolution Image Download MS PowerPoint Slide Multiparameter optimization of a previously identified class of inhibitors of the energy-coupling factor (ECF) transporters enabled the confirmation of in vivo efficacy. ECFs are a class of transmembrane proteins that play a vital role in the active translocation of essential nutrients across cell membranes and are therefore important in the fight against antimicrobial resistance. Aiming to improve the drug-like properties of our inhibitory class, we performed a focused structure–activity relationship study around the Eastern part of our starting molecule 3 by exploiting click chemistry. Our multiparameter optimization resulted in compounds with enhanced metabolic stability and solubility, potent activity against both a panel of Gram-positive bacteria, and against the ECF transporters. We further demonstrate rapid bacterial killing using Enterococcus faecium as a model organism and confirmed in vivo efficacy of the best compounds in Galleria mellonella larvae and Danio rerio (zebrafish) infection models, highlighting the therapeutic potential of our approach.
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