ACS Infectious Diseases · 2019 · 26 citations · 36 references
Life SciencesInfectious DiseasesPharmacologyAntimicrobial ResistanceDrug DiscoveryMedical MicrobiologyAntibacterial ResistanceAntibacterial TherapyAntibiotic ResistanceAntibiotic Resistance MechanismsBeta-lactam ResistanceResistance In Gram-negative BacteriaBeta-lactamase Inhibitor ResistanceBeta-lactamase InhibitorsBeta-lactamase Mediated ResistanceCarbapenem AntibioticsIntrinsic Resistance In Gram-negative BacteriaMultidrug-resistant Gram-negative BacteriaNovel Beta-lactamase Discoveryβ-Lactam Antibiotics
Resistance in Gram-negative bacteria to β-lactam drugs is mediated primarily by the expression of β-lactamases, and co-dosing of β-lactams with a β-lactamase inhibitor (BLI) is a clinically proven strategy to address resistance. New β-lactamases that are not impacted by existing BLIs are spreading and creating the need for development of novel broader spectrum BLIs. IID572 is a novel broad spectrum BLI of the diazabicyclooctane (DBO) class that is able to restore the antibacterial activity of piperacillin against piperacillin/tazobactam-resistant clinical isolates. IID572 is differentiated from other DBOs by its broad inhibition of β-lactamases and the lack of intrinsic antibacterial activity.
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Ryan K. Shields, Brian A. Potoski, Ghady Haidar et al. · Clinical Infectious Diseases · 2016 · 428 citations · Full text