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Rifampicin (R)

University College, London · FDA-approved active Small molecule

Rifampicin inhibits bacterial RNA polymerase, preventing transcription and blocking bacterial protein synthesis.

Rifampicin inhibits bacterial RNA polymerase, preventing transcription and blocking bacterial protein synthesis. Used for Tuberculosis (drug-susceptible and drug-resistant), Leprosy, Atypical mycobacterial infections (MAC, M. marinum).

At a glance

Generic nameRifampicin (R)
Also known asMetronidazole, Rif
SponsorUniversity College, London
Drug classRifamycin antibiotic
TargetBacterial RNA polymerase β-subunit
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Rifampicin binds to the β-subunit of bacterial RNA polymerase II, blocking the path of elongating RNA and preventing transcription initiation. This mechanism is highly selective for bacterial RNA polymerase and has minimal effect on eukaryotic RNA polymerases, making it effective as an antibiotic. It is bactericidal and works against a broad spectrum of gram-positive and gram-negative bacteria.

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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