Valproic Acid

CHEMBL109 Phase 4 Aprobado Small molecule
Half-Life
9-16 hours
Bioavailability
Protein Binding
Molecular Weight
144.2 g/mol
LogP
2.8
Phase
4

This medication is used to treat epilepsy (multiple seizure types), bipolar disorder (as a mood stabilizer), and to prevent migraines. It works by increasing the levels of the calming neurotransmitter GABA in the brain and by stabilizing electrical activity. It must never be taken during pregnancy due to a high risk of birth defects and developmental problems in the baby, and liver function and blood counts require regular monitoring.

Peso molecular

144,2110 g/mol

LogP

2,80

TPSA

37,30 Ų

Regla de cinco de Lipinski

Cumple

Áreas terapéuticas

Clases de fármacos

Mecanismo de acción

Enhances GABA transmission and blocks sodium/calcium channels.

Pharmacokinetics (PK)

Half-Life 9-16 hours

Pharmacodynamics (PD)

Mecanismo

Enhances GABA transmission and blocks sodium/calcium channels.

Estructura 2D

SVG PNG

Cite this structure


                        

Embed this structure


                        

SMILES

CCCC(CCC)C(=O)O

InChI

InChI=1S/C8H16O2/c1-3-5-7(6-4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10)

Molecular Formula

C8H16O2

HBD / HBA

1 / 2

Enlaces Rotables

5

Átomos Pesados

10

No side effects recorded

Side effect data is not yet available for this drug.

Preguntas frecuentes

This medication is used to treat epilepsy (multiple seizure types), bipolar disorder (as a mood stabilizer), and to prevent migraines. It works by increasing the levels of the calming neurotransmitter GABA in the brain and by stabilizing electrical activity. It must never be taken during pregnancy due to a high risk of birth defects and developmental problems in the baby, and liver function and blood counts require regular monitoring.

Enhances GABA transmission and blocks sodium/calcium channels.

Key pharmacokinetic parameters for Valproic Acid: Half-life: 9-16 hours.

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

Related Drugs

{# 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). CHEMBL109. Open-access bioactivity database.
  • PubChem — National Center for Biotechnology Information (NCBI). CID 3121. 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.