Drug intelligence / Profile preview

aztreonam

Development stage
Approved
Lead developer
Bristol Myers Squibb
Modality
Reversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous, Intramuscular, Inhalation
01

Overview

Aztreonam is a synthetic monocyclic beta-lactam antibiotic belonging to the monobactam class. It was originally isolated from Chromobacterium violaceum and is structurally distinct from other beta-lactams such as penicillins and cephalosporins. Aztreonam exhibits potent bactericidal activity against a wide range of aerobic gram-negative bacteria, including Pseudomonas aeruginosa, but has little or no activity against gram-positive bacteria or anaerobes. Its mechanism of action involves binding with high affinity to penicillin-binding protein 3 (PBP3) in susceptible bacteria, thereby inhibiting the final stage of bacterial cell wall synthesis and leading to cell lysis. Aztreonam is highly resistant to many beta-lactamases produced by gram-negative organisms, making it effective even against some multidrug-resistant strains. It is used primarily for severe infections such as those involving the respiratory tract (including pneumonia), urinary tract, blood (bacteremia/sepsis), skin and soft tissue, intra-abdominal area, gynecological sites, bone infections, peritonitis, pelvic inflammatory disease, and for lung infections in cystic fibrosis patients via inhalation[1][2][5][6][9].

Brand names
AzactamCayston
Other names
aztreonam for inhalation solutionaztreonam lysine for inhalation
02

Targets

PBP1A (Penicillin-binding protein 1A)

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