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Terconazole Vaginal Suppository

Hatem AbuHashim · FDA-approved active Small molecule

Terconazole inhibits fungal cell membrane synthesis by blocking lanosterol 14α-demethylase, disrupting ergosterol production in Candida species.

Terconazole inhibits fungal cell membrane synthesis by blocking lanosterol 14α-demethylase, disrupting ergosterol production in Candida species. Used for Vulvovaginal candidiasis (yeast infection).

At a glance

Generic nameTerconazole Vaginal Suppository
Also known asTekangzuo Yindao Shuan
SponsorHatem AbuHashim
Drug classAzole antifungal
TargetLanosterol 14α-demethylase (CYP51)
ModalitySmall molecule
Therapeutic areaInfectious Disease
PhaseFDA-approved

Mechanism of action

Terconazole is an azole antifungal that selectively inhibits the cytochrome P450-dependent enzyme lanosterol 14α-demethylase in fungal cells. This blocks the conversion of lanosterol to ergosterol, a critical component of the fungal cell membrane. The resulting membrane instability and leakage of cellular contents leads to fungal cell death, making it effective against vaginal candidiasis.

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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