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Vancomycin II

Wake Forest University Health Sciences · FDA-approved active Small molecule

Vancomycin II inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors, preventing cross-linking and causing cell wall disruption.

Vancomycin II inhibits bacterial cell wall synthesis by binding to D-Ala-D-Ala peptidoglycan precursors, preventing cross-linking and causing cell wall disruption. Used for Serious gram-positive bacterial infections including methicillin-resistant Staphylococcus aureus (MRSA), Clostridium difficile-associated diarrhea, Endocarditis.

At a glance

Generic nameVancomycin II
Also known asglycopeptide antibiotic
SponsorWake Forest University Health Sciences
Drug classGlycopeptide antibiotic
TargetD-Ala-D-Ala peptidoglycan precursor
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Vancomycin II is a glycopeptide antibiotic that targets the bacterial peptidoglycan layer, a critical structural component of gram-positive bacterial cell walls. By binding to D-alanyl-D-alanine residues on peptidoglycan precursors, it prevents the cross-linking reactions necessary for cell wall integrity. This leads to cell wall instability, leakage of cellular contents, and bacterial cell death.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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