| Literature DB >> 33306385 |
David T Davies1, Simon Leiris1, Magdalena Zalacain1, Nicolas Sprynski1, Jérôme Castandet1, Justine Bousquet1, Clarisse Lozano1, Agustina Llanos1, Laethitia Alibaud1, Srinivas Vasa2, Ramesh Pattipati2, Ravindar Valige2, Bhaskar Kummari2, Srinivasu Pothukanuri2, Cyntia De Piano3, Ian Morrissey3, Kirsty Holden4, Peter Warn4, Francesca Marcoccia5, Manuela Benvenuti6, Cecilia Pozzi6, Giusy Tassone6, Stefano Mangani6, Jean-Denis Docquier5, David Pallin7, Richard Elliot7, Marc Lemonnier1, Martin Everett1.
Abstract
The diazabicyclooctanes (DBOs) are a class of serine β-lactamase (SBL) inhibitors that use a strained urea moiety as the warhead to react with the active serine residue in the active site of SBLs. The first in-class drug, avibactam, as well as several other recently approved DBOs (e.g., relebactam) or those in clinical development (e.g., nacubactam and zidebactam) potentiate activity of β-lactam antibiotics, to various extents, against carbapenem-resistant Enterobacterales (CRE) carrying class A, C, and D SBLs; however, none of these are able to rescue the activity of β-lactam antibiotics against carbapenem-resistant Acinetobacter baumannii (CRAB), a WHO "critical priority pathogen" producing class D OXA-type SBLs. Herein, we describe the chemical optimization and resulting structure-activity relationship, leading to the discovery of a novel DBO, ANT3310, which uniquely has a fluorine atom replacing the carboxamide and stands apart from the current DBOs in restoring carbapenem activity against OXA-CRAB as well as SBL-carrying CRE pathogens.Entities:
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Year: 2020 PMID: 33306385 DOI: 10.1021/acs.jmedchem.0c01535
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446