化学
变构调节
酶
生物化学
抗菌活性
结构-活动关系
生物合成
抗菌剂
立体化学
细菌
化学合成
酶抑制剂
组合化学
虚拟筛选
生物活性
细菌蛋白
药物发现
酶分析
转移酶
蛋白质结构
体外
蛋白质-蛋白质相互作用
蛋白质生物合成
作者
Homero Dominguez-Cisneros,Mohini Mohan Konai,Choon Kim,Neha Rana,Rhona Feltzer,Jeshina Janardhanan,Amr M El-Araby,Van T. Nguyen,Jed F. Fisher,Mayland Chang,Shahriar Mobashery
标识
DOI:10.1021/acs.jmedchem.5c02273
摘要
The allosteric site of penicillin-binding protein 2x (PBP2x), an essential enzyme of cell-wall biosynthesis of Streptococcus pneumoniae, was targeted in virtual screening of >2 M compounds. A benzimidazole-2-methanamine hit emerged, which exhibited a modest minimal-inhibitory concentration (MIC) of 32 mg·L-1. A structure-activity campaign around the structural template resulted in evaluation of 96 compounds, leading to several analogs with MIC of ≤4 mg·L-1. These compounds exhibited a broad-based bactericidal growth inhibition against 31 clinical strains of S. pneumoniae.
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