化学
鲍曼不动杆菌
酶
β-内酰胺酶抑制剂
流出
广谱
抗生素
孔蛋白
丝氨酸
生物化学
细菌
组合化学
大肠杆菌
细菌外膜
铜绿假单胞菌
生物
遗传学
基因
作者
Scott J. Hecker,K. Raja Reddy,Olga Lomovskaya,David C. Griffith,Debora Rubio-Aparicio,Kirk Nelson,Ruslan Tsivkovski,Dongxu Sun,Mojgan Sabet,Ziad Tarazi,Jonathan Parkinson,Maxim Totrov,Serge H. Boyer,Tomasz Glinka,O.A. Pemberton,Yu Chen,Michael N. Dudley
标识
DOI:10.1021/acs.jmedchem.9b01976
摘要
Despite major advances in the β-lactamase inhibitor field, certain enzymes remain refractory to inhibition by agents recently introduced. Most important among these are the class B (metallo) enzyme NDM-1 of Enterobacteriaceae and the class D (OXA) enzymes of Acinetobacter baumannii. Continuing the boronic acid program that led to vaborbactam, efforts were directed toward expanding the spectrum to allow treatment of a wider range of organisms. Through key structural modifications of a bicyclic lead, stepwise gains in spectrum of inhibition were achieved, ultimately resulting in QPX7728 (35). This compound displays a remarkably broad spectrum of inhibition, including class B and class D enzymes, and is little affected by porin modifications and efflux. Compound 35 is a promising agent for use in combination with a β-lactam antibiotic for the treatment of a wide range of multidrug resistant Gram-negative bacterial infections, by both intravenous and oral administration.
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