| Literature DB >> 29627985 |
Krisztina M Papp-Wallace1, Nhu Q Nguyen, Michael R Jacobs2, Christopher R Bethel1, Melissa D Barnes1, Vijay Kumar, Saralee Bajaksouzian2, Susan D Rudin1, Philip N Rather3,4, Satish Bhavsar5, Tadiparthi Ravikumar5, Prasad K Deshpande5, Vijay Patil5, Ravindra Yeole5, Sachin S Bhagwat5, Mahesh V Patel5, Focco van den Akker, Robert A Bonomo1.
Abstract
Limited treatment options exist to combat infections caused by multidrug-resistant (MDR) Gram-negative bacteria possessing broad-spectrum β-lactamases. The design of novel β-lactamase inhibitors is of paramount importance. Here, three novel diazabicyclooctanes (DBOs), WCK 5153, zidebactam (WCK 5107), and WCK 4234 (compounds 1-3, respectively), were synthesized and biochemically characterized against clinically important bacteria. Compound 3 inhibited class A, C, and D β-lactamases with unprecedented k2/ K values against OXA carbapenemases. Compounds 1 and 2 acylated class A and C β-lactamses rapidly but not the tested OXAs. Compounds 1-3 formed highly stable acyl-complexes as demonstrated by mass spectrometry. Crystallography revealed that 1-3 complexed with KPC-2 adopted a "chair conformation" with the sulfate occupying the carboxylate binding region. The cefepime-2 and meropenem-3 combinations were effective in murine peritonitis and neutropenic lung infection models caused by MDR Acinetobacter baumannii. Compounds 1-3 are novel β-lactamase inhibitors that demonstate potent cross-class inhibition, and clinical studies targeting MDR infections are warranted.Entities:
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Year: 2018 PMID: 29627985 PMCID: PMC6131718 DOI: 10.1021/acs.jmedchem.8b00091
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446