阴沟肠杆菌
结构异构体
药品
化学
药理学
生物
立体化学
生物化学
肠杆菌科
大肠杆菌
基因
作者
Yvonne Fu Zi Chan,Yvonne Peijun Zhou,Ban Hock Tan,Candice Yuen Yue Chan,Benjamin Pei Zhi Cherng,Yii Ean Teh,Gee Chuan Wong,Andrea Lay‐Hoon Kwa,Tze Peng Lim,Kelvin Kau Kiat Goh,Farah Iffah Binte Zulkifli,Shimin Jasmine Chung
标识
DOI:10.1016/j.ijantimicag.2023.106748
摘要
The regioisomers of the anandamide-acting drug LY2183240 exhibited specific potent and competitive inhibitory activities against class C β-lactamases. More explicitly, the 1,5- and 2,5-regioisomers inhibited AmpC from Enterobacter hormaechei (formerly Enterobacter cloacae) with inhibitor binding affinity values of 1.8 µM and 2.45 µM, respectively. Structural molecular modelling studies revealed the interaction of the regioisomers with the relevant residues of the catalytic site of cephalosporinase from E. hormaechei P99, which included Tyr150, Lys315 and Thr316.
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