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Cited by 422

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Discovery of a Cyclic Boronic Acid β-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases

Open access
Hecker, Scott J., Reddy, K. Raja, Totrov, Maxim, Hirst, Gavin C., Lomovskaya, Olga, Griffith, David C., King, Paula, Tsivkovski, Ruslan, Sun, Dongxu, Sabet, Mojgan, Tarazi, Ziad, Clifton, Matthew C., Atkins, Kateri, Raymond, Amy, Potts, Kristy T., Abendroth, Jan, Boyer, Serge H., Loutit, Jeffrey S., Morgan, Elizabeth E., Durso, Stephanie, Dudley, Michael N.·2015·Journal of Medicinal Chemistry

Abstract

The increasing dissemination of carbapenemases in Gram-negative bacteria has threatened the clinical usefulness of the β-lactam class of antimicrobials. A program was initiated to discover a new series of serine β-lactamase inhibitors containing a boronic acid pharmacophore, with the goal of finding a potent inhibitor of serine carbapenemase enzymes that are currently compromising the utility of the carbapenem class of antibacterials. Potential lead structures were screened in silico by modeling into the active sites of key serine β-lactamases. Promising candidate molecules were synthesized and evaluated in biochemical and whole-cell assays. Inhibitors were identified with potent inhibition of serine carbapenemases, particularly the Klebsiella pneumoniae carbapenemase (KPC), with no inhibition of mammalian serine proteases. Studies in vitro and in vivo show that RPX7009 (9f) is a broad-spectrum inhibitor, notably restoring the activity of carbapenems against KPC-producing strains. Combined with a carbapenem, 9f is a promising product for the treatment of multidrug resistant Gram-negative bacteria.

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Metadata

Authors
Hecker, S. J., Reddy, K. R., Totrov, M., Hirst, G. C., Lomovskaya, O., Griffith, D. C., King, P., Tsivkovski, R., Sun, D., Sabet, M., Tarazi, Z., Clifton, M. C., Atkins, K., Raymond, A., Potts, K. T., Abendroth, J., Boyer, S. H., Loutit, J. S., Morgan, E. E., Durso, S., & Dudley, M. N.
Venue
Journal of Medicinal Chemistry
Published
2015-03-17
Volume
58
Issue
9
Pages
3682-3692
ISSN
  • 0022-2623 (ISSN-L)
  • 1520-4804
OpenAlex
W1968310807
Cited by
422
References
25
Type
other
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Discovery of a Cyclic Boronic Acid β-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases. https://app.cochat.ai/papers/10.1021/acs.jmedchem.5b00127
The paper
Hecker, S. J., Reddy, K. R., Totrov, M., Hirst, G. C., Lomovskaya, O., Griffith, D. C., King, P., Tsivkovski, R., Sun, D., Sabet, M., Tarazi, Z., Clifton, M. C., Atkins, K., Raymond, A., Potts, K. T., Abendroth, J., Boyer, S. H., Loutit, J. S., Morgan, E. E., . . . Dudley, M. N. (2015). Discovery of a Cyclic Boronic Acid β-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases. Journal of Medicinal Chemistry. https://doi.org/10.1021/acs.jmedchem.5b00127

Data sources

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.