Drug intelligence / Profile preview

azlocillin

Development stage
Discontinued
Lead developer
Bayer
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
01

Overview

Azlocillin is a semisynthetic, extended-spectrum acylampicillin antibiotic belonging to the ureidopenicillin subclass of beta-lactam antibiotics. It acts by binding to penicillin-binding proteins (PBPs) within the bacterial cell wall, thereby inhibiting the final stage of peptidoglycan cross-linking essential for bacterial cell wall synthesis. This leads to cell lysis mediated by autolytic enzymes such as autolysins and may also involve disruption of an autolysin inhibitor[1][2][5][7][8]. Azlocillin exhibits broad-spectrum antibacterial activity against both gram-negative and gram-positive organisms, including *Pseudomonas aeruginosa*, *Escherichia coli*, *Haemophilus influenzae*, *Streptococcus* spp., *Enterococcus* spp., *Listeria monocytogenes*, *Proteus mirabilis*, *Salmonella* spp., and *Shigella* spp.[2][5][8]. It was primarily used for severe infections caused by susceptible bacteria but is no longer marketed in some regions[5].

Brand names
Azlin
Other names
azlocillin sodiumazlocillin sodium salt
02

Targets

PBP (Penicillin-binding protein family)

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