The escalating threat of antibiotic resistance, driven largely by the spread of β-lactamase enzymes, necessitates innovative therapeutic strategies. This work investigates the potential of a novel class of boronic acid-phosphonic acid anhydrides as β-lactamase inhibitors, as well as their oxidative stability and diol-binding ability. Evaluation of two lead compounds, 6 and 12, demonstrated potent inhibition of multiple classes of β-lactamases. Compound 12 was found to be particularly effective, potently inhibiting a broad panel of β-lactamases, including KPC-2 and GC-1, with sustained activity at low micromolar concentrations. These results establish the boronic acid-phosphonic acid anhydride scaffold as a promising and versatile platform for the development of new β-lactamase inhibitors. This discovery provides a valuable foundation for future efforts to combat antibiotic-resistant bacterial infections through rational drug design.
Building similarity graph...
Analyzing shared references across papers
Loading...
Ospanow et al. (Sat,) studied this question.
synapsesocial.com/papers/69a67dd6f353c071a6f09cfa — DOI: https://doi.org/10.1021/acs.joc.5c02782
Elisa Ospanow
Mirele Barsoum
Carol A. Tanner
The Journal of Organic Chemistry
University of Waterloo
Dalhousie University
University of Prince Edward Island
Building similarity graph...
Analyzing shared references across papers
Loading...