Acrisorcin

CHEMBL1201038 Phase 4 承認済み Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
388.5 g/mol
LogP
Phase
4

A topical antifungal agent used historically to treat tinea versicolor, a fungal skin infection that causes patches of discolored skin on the trunk and shoulders. It works by disrupting the cell membrane of the yeast responsible for the infection. It is rarely used today, having been largely supplanted by more effective and better-tolerated topical and oral antifungal treatments.

分子量

388.5000 g/mol

TPSA

79.40 Ų

作用機序

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

機序

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

2D構造

SVG PNG

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SMILES

CCCCCCc1ccc(O)cc1O.Nc1c2ccccc2nc2ccccc12

InChI

InChI=1S/C13H10N2.C12H18O2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13;1-2-3-4-5-6-10-7-8-11(13)9-12(10)14/h1-8H,(H2,14,15);7-9,13-14H,2-6H2,1H3

Molecular Formula

C25H28N2O2

HBD / HBA

3 / 4

回転可能結合数

5

重原子数

29

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

A topical antifungal agent used historically to treat tinea versicolor, a fungal skin infection that causes patches of discolored skin on the trunk and shoulders. It works by disrupting the cell membrane of the yeast responsible for the infection. It is rarely used today, having been largely supplanted by more effective and better-tolerated topical and oral antifungal treatments.

Applied directly to the skin or mucous membranes, where it exerts its therapeutic effect locally at the site of application with minimal systemic absorption.

Yes, Acrisorcin 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). CHEMBL1201038. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 24144. 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.