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Molecular Insights on the Release of Avibactam from the Acyl-Enzyme Complex
Structural insight into potent broad-spectrum inhibition with reversible recyclization mechanism: avibactam in complex with CTX-M-15 and Pseudomonas aeruginosa AmpC β-lactamases. - Abstract - Europe PMC
Avibactam | C7H11N3O6S | CID 9835049 - PubChem
A theoretical approach for the acylation/deacylation mechanisms of avibactam in the reversible inhibition of KPC-2 | SpringerLink
Inhibitors of b-Lactamases. New Life of b-Lactam Antibiotics
First oral antibiotic booster for four decades could tackle drug resistance | Research | Chemistry World
Epidemiology and Mechanisms of Ceftazidime–Avibactam Resistance in Gram-Negative Bacteria - ScienceDirect
Avibactam - an overview | ScienceDirect Topics
Schematic diagram of avibactam inhibition and deacylation pathways of... | Download Scientific Diagram
Pharmacological aspects and spectrum of action of ceftazidime–avibactam: a systematic review | SpringerLink
Avibactam is a covalent, reversible, non–β-lactam β-lactamase inhibitor | PNAS
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 sodium | 99.97%(HPLC) | In Stock | β-lactamase inhibitor
Ceftazidime/avibactam - Wikipedia
Avibactam and Class C β-Lactamases: Mechanism of Inhibition, Conservation of the Binding Pocket, and Implications for Resistance | Antimicrobial Agents and Chemotherapy
Avibactam | Uses, Brand Names, Mechanism Of Action
Investigations on recyclisation and hydrolysis in avibactam mediated serine β-lactamase inhibition - Organic & Biomolecular Chemistry (RSC Publishing) DOI:10.1039/C6OB00353B
Unexpected Challenges in Treating Multidrug-Resistant Gram-Negative Bacteria: Resistance to Ceftazidime-Avibactam in Archived Isolates of Pseudomonas aeruginosa | Antimicrobial Agents and Chemotherapy