Molecular Insights on the Release of Avibactam from the Acyl-Enzyme Complex
Unexpected Challenges in Treating Multidrug-Resistant Gram-Negative Bacteria: Resistance to Ceftazidime-Avibactam in Archived Isolates of Pseudomonas aeruginosa | Antimicrobial Agents and Chemotherapy
Interplay between β-lactamases and new β-lactamase inhibitors | Nature Reviews Microbiology
CARIOU Kevin on Twitter: "Very happy to share that our first paper of 2020 is out! A review in @OrgBiomolChem on the synthesis of avibactam and other diazabicyclooctane β-lactamase inhibitors. Congrats to
Ceftazidime/avibactam - Wikipedia
A theoretical approach for the acylation/deacylation mechanisms of avibactam in the reversible inhibition of KPC-2 | SpringerLink
Avibactam is a covalent, reversible, non–β-lactam β-lactamase inhibitor | PNAS
Molecular Mechanism of Avibactam-Mediated β-Lactamase Inhibition. | Semantic Scholar
Molecular Mechanism of Avibactam-Mediated β-Lactamase Inhibition | ACS Infectious Diseases
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The road to avibactam: the first clinically useful non-β-lactam working somewhat like a β-lactam | Future Medicinal Chemistry
Inhibitors of b-Lactamases. New Life of b-Lactam Antibiotics
Molecular insights into avibactam mediated class C β-lactamase inhibition: competition between reverse acylation and hydrolysis through desulfation - Physical Chemistry Chemical Physics (RSC Publishing) DOI:10.1039/C8CP01670D
Avibactam | C7H11N3O6S | CID 9835049 - PubChem
Ceftazidime/avibactam - Wikipedia
Antibiotics | Free Full-Text | The Revival of Aztreonam in Combination with Avibactam against Metallo-β-Lactamase-Producing Gram-Negatives: A Systematic Review of In Vitro Studies and Clinical Cases