| Literature DB >> 32786279 |
David T Davies1, Simon Leiris1, Nicolas Sprynski1, Jérôme Castandet1, Clarisse Lozano1, Justine Bousquet1, Magdalena Zalacain1, Srinivas Vasa2, Praveen K Dasari2, Ramesh Pattipati2, Naresh Vempala2, Swetha Gujjewar2, SyamKumar Godi2, Raju Jallala2, Rajashekar Reddy Sathyap2, Narasimha A Darshanoju2, Vengala R Ravu2, Ramakrishna R Juventhala2, Narender Pottabathini2, Somesh Sharma2, Srinivasu Pothukanuri2, Kirsty Holden3, Peter Warn3, Francesca Marcoccia4, Manuela Benvenuti5, Cecilia Pozzi5, Stefano Mangani5, Jean-Denis Docquier4, Marc Lemonnier1, Martin Everett1.
Abstract
The clinical effectiveness of the important β-lactam class of antibiotics is under threat by the emergence of resistance, mostly due to the production of acquired serine- (SBL) and metallo-β-lactamase (MBL) enzymes. To address this resistance issue, multiple β-lactam/β-lactamase inhibitor combinations have been successfully introduced into the clinic over the past several decades. However, all of those combinations contain SBL inhibitors and, as yet, there are no MBL inhibitors in clinical use. Consequently, there exists an unaddressed yet growing healthcare problem due to the rise in recent years of highly resistant strains which produce New Delhi metallo (NDM)-type metallo-carbapenemases. Previously, we reported the characterization of an advanced MBL inhibitor lead compound, ANT431. Herein, we discuss the completion of a lead optimization campaign culminating in the discovery of the preclinical candidate ANT2681, a potent NDM inhibitor with strong potential for clinical development.Entities:
Keywords: ANT2681; New Delhi metallo-β-lactamase (NDM); antibiotic resistance; carbapenem-resistant Enterobacteriaceae; meropenem; metallo-β-lactamase inhibitor
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Year: 2020 PMID: 32786279 DOI: 10.1021/acsinfecdis.0c00207
Source DB: PubMed Journal: ACS Infect Dis ISSN: 2373-8227 Impact factor: 5.084