Butoconazole

CHEMBL1295 Phase 4 Approved Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
411.8 g/mol
LogP
6.4
Phase
4

An azole antifungal used as a vaginal cream to treat vaginal yeast infections caused by Candida species. It works by inhibiting ergosterol synthesis, disrupting the fungal cell membrane. A single-dose formulation provides convenience for treatment of uncomplicated vaginal candidiasis.

Molecular Weight

411.8000 g/mol

LogP

6.40

TPSA

43.10 Ų

Lipinski RO5

Pass

Mechanism of Action

Inhibits the fungal cytochrome P450 enzyme lanosterol 14-alpha-demethylase, blocking ergosterol synthesis essential for fungal cell membrane integrity.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mechanism

Inhibits the fungal cytochrome P450 enzyme lanosterol 14-alpha-demethylase, blocking ergosterol synthesis essential for fungal cell membrane integrity.

2D Structure

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

Clc1ccc(CCC(Cn2ccnc2)Sc2c(Cl)cccc2Cl)cc1

InChI

InChI=1S/C19H17Cl3N2S/c20-15-7-4-14(5-8-15)6-9-16(12-24-11-10-23-13-24)25-19-17(21)2-1-3-18(19)22/h1-5,7-8,10-11,13,16H,6,9,12H2

Molecular Formula

C19H17Cl3N2S

HBD / HBA

- / 2

Rotatable Bonds

7

Heavy Atoms

25

No targets recorded

Target interaction data is not yet available for this drug.

No interactions recorded

Drug interaction data is not yet available for this compound.

No side effects recorded

Side effect data is not yet available for this drug.

Frequently Asked Questions

An azole antifungal used as a vaginal cream to treat vaginal yeast infections caused by Candida species. It works by inhibiting ergosterol synthesis, disrupting the fungal cell membrane. A single-dose formulation provides convenience for treatment of uncomplicated vaginal candidiasis.

Inhibits the fungal cytochrome P450 enzyme lanosterol 14-alpha-demethylase, blocking ergosterol synthesis essential for fungal cell membrane integrity.

Yes, Butoconazole is an approved drug. It has reached clinical phase 4. It is classified as a Small molecule.

{# References & Data Sources section for drug detail pages. Renders standard pharmacological database links plus the drug's data_sources field. #}

References & Data Sources

  • ChEMBL — European Bioinformatics Institute (EBI). CHEMBL1295. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 47472. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-04.

Medical Disclaimer

This content is for educational and informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult a qualified healthcare provider before making medication decisions.

Data sources: ChEMBL, PubChem, DailyMed.