Butoconazole

CHEMBL1295 Phase 4 承認済み 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.

分子量

411.8000 g/mol

LogP

6.40

TPSA

43.10 Ų

リピンスキーの五則

適合

作用機序

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

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

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

2D構造

SVG PNG

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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

回転可能結合数

7

重原子数

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.

よくある質問

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.

医学的免責事項

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.