| Literature DB >> 32150407 |
Scott J Hecker1, K Raja Reddy1, Olga Lomovskaya1, David C Griffith1, Debora Rubio-Aparicio1, Kirk Nelson1, Ruslan Tsivkovski1, Dongxu Sun1, Mojgan Sabet1, Ziad Tarazi1, Jonathan Parkinson1, Maxim Totrov2, Serge H Boyer1, Tomasz W Glinka1, Orville A Pemberton3, Yu Chen3, Michael N Dudley1.
Abstract
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.Entities:
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Year: 2020 PMID: 32150407 DOI: 10.1021/acs.jmedchem.9b01976
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446