Prasterone

CHEMBL90593 Phase 4 Disetujui Small molecule
Half-Life
Bioavailability
Protein Binding
Molecular Weight
288.4 g/mol
LogP
3.2
Phase
4

Prasterone (dehydroepiandrosterone, DHEA) is an endogenous steroid hormone and neurosteroid precursor that is peripherally converted to androgens and estrogens in target tissues, and also acts as a GABA receptor antagonist and NMDA receptor agonist. It is approved for the treatment of moderate-to-severe dyspareunia associated with vulvar and vaginal atrophy in postmenopausal women, and is under investigation for various other conditions.

Berat Molekul

288,4000 g/mol

LogP

3,20

TPSA

37,30 Ų

Lipinski RO5

Lulus

Area Terapeutik

Mekanisme Kerja

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Pharmacokinetics (PK)

Pharmacodynamics (PD)

Mekanisme

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Struktur 2D

SVG PNG

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SMILES

C[C@]12CC[C@H](O)CC1=CC[C@@H]1[C@@H]2CC[C@]2(C)C(=O)CC[C@@H]12

InChI

InChI=1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h3,13-16,20H,4-11H2,1-2H3/t13-,14-,15-,16-,18-,19-/m0/s1

Molecular Formula

C19H28O2

HBD / HBA

1 / 2

Ikatan yang Dapat Dirotasi

0

Atom Berat

21

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.

Pertanyaan yang Sering Diajukan

Prasterone (dehydroepiandrosterone, DHEA) is an endogenous steroid hormone and neurosteroid precursor that is peripherally converted to androgens and estrogens in target tissues, and also acts as a GABA receptor antagonist and NMDA receptor agonist. It is approved for the treatment of moderate-to-severe dyspareunia associated with vulvar and vaginal atrophy in postmenopausal women, and is under investigation for various other conditions.

Binds to and activates its target receptor, mimicking the action of the endogenous ligand to produce a specific physiological response.

Yes, Prasterone 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). CHEMBL90593. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 5881. Chemical information database.

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

Penyangkalan Medis

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.