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Valproic acid, sodium salt

Sanofi · FDA-approved active Small molecule

Valproic acid inhibits histone deacetylases and enhances GABA neurotransmission, leading to increased inhibitory signaling in the central nervous system.

Valproic acid inhibits histone deacetylases and enhances GABA neurotransmission, leading to increased inhibitory signaling in the central nervous system. Used for Epilepsy and seizure disorders, Bipolar disorder (acute mania), Migraine prophylaxis.

At a glance

Generic nameValproic acid, sodium salt
SponsorSanofi
Drug classHistone deacetylase inhibitor; anticonvulsant; mood stabilizer
TargetHistone deacetylase (HDAC); GABA metabolism
ModalitySmall molecule
Therapeutic areaNeurology; Psychiatry; Oncology
PhaseFDA-approved

Mechanism of action

Valproic acid (sodium salt) works through multiple mechanisms: it inhibits histone deacetylase enzymes, which increases histone acetylation and alters gene expression; it also increases brain levels of GABA, an inhibitory neurotransmitter, by enhancing its synthesis and reducing its catabolism. These combined effects produce anticonvulsant, mood-stabilizing, and neuroprotective properties.

Approved indications

Common side effects

Key clinical trials

Primary sources

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

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