Physician Data Query

Last uploaded: January 31, 2024
Preferred Name

divalproex sodium

Synonyms

sodium divalproex

Depakote

Depacon

Valparin

sodium hydrogen bis(2-propylpentanoate)

Epilex

valproate semisodium

Abbott 50711

Depakote ER

Epival

Definitions

A stable coordination compound comprised of sodium valproate and valproic acid with anticonvulsant and antiepileptic activities. Divalproex dissociates to the valproate ion in the gastrointestinal tract. This agent binds to and inhibits gamma-aminobutyric acid (GABA) transaminase and its anticonvulsant activity may be exerted by increasing brain concentration of GABA and by inhibiting enzymes that catabolize GABA or block the reuptake of GABA into glia and nerve endings. Divalproex may also work by suppressing repetitive neuronal firing through inhibition of voltage-sensitive sodium channels. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C28996" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C28996" NCI Thesaurus)

ID

http://purl.bioontology.org/ontology/PDQ/CDR0000778070

altLabel

sodium divalproex

Depakote

Depacon

Valparin

sodium hydrogen bis(2-propylpentanoate)

Epilex

valproate semisodium

Abbott 50711

Depakote ER

Epival

CAS Registry

76584-70-8

cui

C2987577

C2699792

C2699791

C0939309

C2987459

C0719750

C0886883

C0719751

DATE FIRST PUBLISHED

2016-01-14

Date last modified

2016-01-14

definition

A stable coordination compound comprised of sodium valproate and valproic acid with anticonvulsant and antiepileptic activities. Divalproex dissociates to the valproate ion in the gastrointestinal tract. This agent binds to and inhibits gamma-aminobutyric acid (GABA) transaminase and its anticonvulsant activity may be exerted by increasing brain concentration of GABA and by inhibiting enzymes that catabolize GABA or block the reuptake of GABA into glia and nerve endings. Divalproex may also work by suppressing repetitive neuronal firing through inhibition of voltage-sensitive sodium channels. Check for "https://www.cancer.gov/about-cancer/treatment/clinical-trials/intervention/C28996" active clinical trials using this agent. ("http://ncit.nci.nih.gov/ncitbrowser/ConceptReport.jsp?dictionary=NCI%20Thesaurus&code=C28996" NCI Thesaurus)

LT

TRD

NCI ID

C28996

notation

CDR0000778070

ORIG STY

Drug/agent

prefLabel

divalproex sodium

tui

T109

T121

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