Last reviewed · How we verify

Divalproex Sodium (Depakote)

National Institute on Drug Abuse (NIDA) · Phase 3 active Small molecule

Divalproex sodium inhibits histone deacetylase and enhances GABA neurotransmission, stabilizing neuronal membranes and reducing abnormal electrical activity in the brain.

Divalproex sodium inhibits histone deacetylase and enhances GABA neurotransmission, stabilizing neuronal membranes and reducing abnormal electrical activity in the brain. Used for Epilepsy (seizure disorders), Bipolar disorder (acute mania), Migraine prophylaxis.

At a glance

Generic nameDivalproex Sodium (Depakote)
SponsorNational Institute on Drug Abuse (NIDA)
Drug classHistone deacetylase inhibitor; anticonvulsant; mood stabilizer
TargetHistone deacetylase; GABA metabolism; sodium channels
ModalitySmall molecule
Therapeutic areaNeurology; Psychiatry
PhasePhase 3

Mechanism of action

Divalproex is a compound of sodium valproate and valproic acid that works through multiple mechanisms: it increases brain levels of GABA (an inhibitory neurotransmitter) by inhibiting its degradation, blocks sodium channels to reduce neuronal excitability, and inhibits histone deacetylase enzymes which affects gene expression. These combined effects make it effective for conditions characterized by abnormal neuronal firing or mood dysregulation.

Approved indications

Common side effects

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results