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Clotrimazole 1%

Jinnah Postgraduate Medical Centre · FDA-approved active Small molecule

Clotrimazole inhibits fungal cell membrane synthesis by blocking the conversion of lanosterol to ergosterol via inhibition of fungal cytochrome P450 enzymes.

Clotrimazole inhibits fungal cell membrane synthesis by blocking the conversion of lanosterol to ergosterol via inhibition of fungal cytochrome P450 enzymes. Used for Topical fungal infections (dermatophytes, Candida, Malassezia), Vaginal candidiasis, Oropharyngeal candidiasis.

At a glance

Generic nameClotrimazole 1%
SponsorJinnah Postgraduate Medical Centre
Drug classImidazole antifungal
TargetFungal cytochrome P450 (lanosterol 14α-demethylase)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Clotrimazole is an imidazole antifungal that disrupts the synthesis of ergosterol, a critical component of fungal cell membranes. By inhibiting the fungal enzyme lanosterol 14α-demethylase (a cytochrome P450 enzyme), it causes accumulation of toxic sterol precursors and membrane instability, leading to fungal cell death. This mechanism is selective for fungal cells over human cells due to structural differences in sterol synthesis pathways.

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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