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Cefazolin / Vancomycin

University of Cincinnati · FDA-approved active Small molecule

Cefazolin and vancomycin are bactericidal antibiotics that inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins and D-Ala-D-Ala residues, respectively.

Cefazolin and vancomycin are bactericidal antibiotics that inhibit bacterial cell wall synthesis by binding to penicillin-binding proteins and D-Ala-D-Ala residues, respectively. Used for Surgical site infection prophylaxis, Serious gram-positive bacterial infections, Methicillin-resistant Staphylococcus aureus (MRSA) infections.

At a glance

Generic nameCefazolin / Vancomycin
Also known asAncef, Vancin
SponsorUniversity of Cincinnati
Drug classBeta-lactam antibiotic / Glycopeptide antibiotic
TargetPenicillin-binding proteins / D-Ala-D-Ala peptidoglycan precursors
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Cefazolin is a first-generation cephalosporin that inhibits cross-linking of peptidoglycan in the bacterial cell wall. Vancomycin is a glycopeptide antibiotic that binds to D-Ala-D-Ala precursors and prevents cell wall synthesis. Together, this combination provides broad-spectrum coverage against gram-positive bacteria and is commonly used for surgical prophylaxis and serious infections.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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