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Clotrimazole Troche

Weill Medical College of Cornell University · FDA-approved active Small molecule

Clotrimazole inhibits fungal cell membrane ergosterol synthesis by blocking lanosterol 14α-demethylase, disrupting membrane integrity and causing fungal cell death.

Clotrimazole inhibits fungal cell membrane ergosterol synthesis by blocking lanosterol 14α-demethylase, disrupting membrane integrity and causing fungal cell death. Used for Oropharyngeal candidiasis (oral thrush).

At a glance

Generic nameClotrimazole Troche
Also known asMycelex
SponsorWeill Medical College of Cornell University
Drug classAzole antifungal
TargetLanosterol 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Clotrimazole is an azole antifungal that selectively inhibits the cytochrome P450-dependent enzyme lanosterol 14α-demethylase in fungi. This blocks the conversion of lanosterol to ergosterol, a critical component of the fungal cell membrane. The resulting depletion of ergosterol and accumulation of toxic sterol precursors leads to increased membrane permeability and fungal cell lysis.

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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