Drug intelligence / Profile preview

cefoperazone-sulbactam + ciprofloxacin

Development stage
Unknown
Lead developer
Bayer
Modality
Irreversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules, Reversible Covalent Inhibitors → Covalent Small Molecules → Small Molecules
Administration
Intravenous, Intramuscular, Oral
01

Overview

Cefoperazone-sulbactam + ciprofloxacin is a combination therapy consisting of two antibiotics (cefoperazone and ciprofloxacin) and a beta-lactamase inhibitor (sulbactam). Cefoperazone is a third-generation cephalosporin antibiotic that inhibits bacterial cell wall synthesis. Sulbactam is a beta-lactamase inhibitor that protects cefoperazone from enzymatic degradation by beta-lactamase-producing bacteria, thereby extending its spectrum of activity[8]. Ciprofloxacin is a second-generation fluoroquinolone antibiotic that inhibits bacterial DNA gyrase and topoisomerase IV, enzymes essential for DNA replication[6]. This combination may be used in clinical settings to treat severe or resistant infections caused by susceptible gram-negative and some gram-positive organisms, including multidrug-resistant strains. The rationale for combining these agents includes broadening the antibacterial spectrum, overcoming resistance mechanisms (such as beta-lactamases), and achieving potential synergistic effects against difficult-to-treat pathogens[1][2][8].

Other names
cefoperazone plus sulbactam and ciprofloxacincefoperazone/sulbactam + ciprofloxacin
02

Targets

β-lactamaseTopo IV (Bacterial Topoisomerase IV)DNA gyrasePBP (Penicillin-binding protein family)

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