Trilostane

CHEMBL1200907 Phase 4 Aprobado Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
329.4 g/mol
LogP
2.9
Phase
4

Trilostane is a synthetic steroid analog that inhibits 3-beta-hydroxysteroid dehydrogenase, an enzyme critical for adrenal steroidogenesis, thereby reducing production of cortisol, aldosterone, and other steroids. It is used primarily in veterinary medicine to treat hyperadrenocorticism (Cushing's disease) and has been investigated in humans for adrenal-dependent conditions including certain hormone-sensitive cancers. Its adrenosuppressive action makes it relevant in prostate cancer research due to androgen pathway interference.

Peso molecular

329,4000 g/mol

LogP

2,90

TPSA

76,80 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Estructura 2D

SVG PNG

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SMILES

C[C@]12CC[C@H]3[C@@H](CC[C@@]45O[C@@H]4C(O)=C(C#N)C[C@]35C)[C@@H]1CC[C@@H]2O

InChI

InChI=1S/C20H27NO3/c1-18-7-6-14-12(13(18)3-4-15(18)22)5-8-20-17(24-20)16(23)11(10-21)9-19(14,20)2/h12-15,17,22-23H,3-9H2,1-2H3/t12-,13-,14-,15-,17+,18-,19+,20+/m0/s1

Molecular Formula

C20H27NO3

HBD / HBA

2 / 4

Enlaces Rotables

0

Átomos Pesados

24

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.

Preguntas frecuentes

Trilostane is a synthetic steroid analog that inhibits 3-beta-hydroxysteroid dehydrogenase, an enzyme critical for adrenal steroidogenesis, thereby reducing production of cortisol, aldosterone, and other steroids. It is used primarily in veterinary medicine to treat hyperadrenocorticism (Cushing's disease) and has been investigated in humans for adrenal-dependent conditions including certain hormone-sensitive cancers. Its adrenosuppressive action makes it relevant in prostate cancer research due to androgen pathway interference.

Yes, Trilostane 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). CHEMBL1200907. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 656583. Chemical information database.

Data aggregated from publicly available pharmacological databases. Last updated 2026-03-28.

Aviso médico

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.