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Details

Stereochemistry ACHIRAL
Molecular Formula 2C8H15O2.Mg
Molecular Weight 310.7127
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALPROATE MAGNESIUM

SMILES

CCCC(CCC)C(=O)[O-].CCCC(CCC)C(=O)[O-].[Mg+2]

InChI

InChIKey=LKLLHOIUJVEAGU-UHFFFAOYSA-L
InChI=1S/2C8H16O2.Mg/c2*1-3-5-7(6-4-2)8(9)10;/h2*7H,3-6H2,1-2H3,(H,9,10);/q;;+2/p-2

HIDE SMILES / InChI

Description
Curator's Comment:: http://psychopharmacologyinstitute.com/mood-stabilizers/valproate-in-psychiatry-approved-indications-and-off-label-uses/ | https://www.accessdata.fda.gov/drugsatfda_docs/label/2009/022152s002lbl.pdf | https://www.ncbi.nlm.nih.gov/pubmed/12847559 | https://www.ncbi.nlm.nih.gov/pubmed/11742974 | https://www.ncbi.nlm.nih.gov/pubmed/11473107

The mechanisms of VPA which seem to be of clinical importance in the treatment of epilepsy include increased gamma-aminobutyric acid (GABA)-ergic activity, reduction in excitatory neurotransmission, and modification of monoamines. Recently, it was discovered that the VPA is a class I selective histone deacetylase inhibitor. This activity can be distinguished from its therapeutically exploited antiepileptic activity.

Originator

Sources: Burton B.S. (1882) On the propyl derivatives and decomposition products of ethylacetoacetate. Am Chem J3: 385–395
Curator's Comment:: reference retrieved from https://link.springer.com/chapter/10.1007%2F978-3-0348-8759-5_1

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
DEPAKENE

Approved Use

Depakene (valproic acid) is indicated as monotherapy and adjunctive therapy in the treatment of patients with complex partial seizures that occur either in isolation or in association with other types of seizures. Depakene (valproic acid) is indicated for use as sole and adjunctive therapy in the treatment of simple and complex absence seizures, and adjunctively in patients with multiple seizure types which include absence seizures. Simple absence is defined as very brief clouding of the sensorium or loss of consciousness accompanied by certain generalized epileptic discharges without other detectable clinical signs. Complex absence is the term used when other signs are also present.
Preventing
STAVZOR

Approved Use

Stavzor (valproic acid) delayed release capsules is indicated for: • Acute treatment of manic episodes associated with bipolar disorder • Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absence seizures • Prophylaxis of migraine headaches

Launch Date

1217203200000
Primary
STAVZOR

Approved Use

Stavzor (valproic acid) delayed release capsules is indicated for: • Acute treatment of manic episodes associated with bipolar disorder • Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include absence seizures • Prophylaxis of migraine headaches

Launch Date

1217203200000
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
107.2 mg/L
500 mg 2 times / day multiple, oral
dose: 500 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
VALPROIC ACID plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: FEMALE / MALE
food status: FED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
1951 mg × h/L
500 mg 2 times / day multiple, oral
dose: 500 mg
route of administration: Oral
experiment type: MULTIPLE
co-administered:
VALPROIC ACID plasma
Homo sapiens
population: HEALTHY
age: UNKNOWN
sex: FEMALE / MALE
food status: FED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
16 h
1000 mg 1 times / day steady-state, oral
dose: 1000 mg
route of administration: Oral
experiment type: STEADY-STATE
co-administered:
VALPROIC ACID unknown
Homo sapiens
population: UNKNOWN
age: UNKNOWN
sex: UNKNOWN
food status: UNKNOWN
Doses

Doses

DosePopulationAdverse events​
150 mg/kg single, intravenous
Highest studied dose
Dose: 150 mg/kg
Route: intravenous
Route: single
Dose: 150 mg/kg
Sources:
healthy, 30.2 ± 11.7
Health Status: healthy
Age Group: 30.2 ± 11.7
Sex: M+F
Sources:
DLT: Headache, Nausea...
Dose limiting toxicities:
Headache
Nausea
Sources:
140 mg/kg single, intravenous
MTD
Dose: 140 mg/kg
Route: intravenous
Route: single
Dose: 140 mg/kg
Sources:
healthy, 30.2 ± 11.7
Health Status: healthy
Age Group: 30.2 ± 11.7
Sex: M+F
Sources:
25 g single, oral
Overdose
Dose: 25 g
Route: oral
Route: single
Dose: 25 g
Sources:
unhealthy, 37
Health Status: unhealthy
Age Group: 37
Sex: M
Sources:
Disc. AE: Somnolence...
AEs leading to
discontinuation/dose reduction:
Somnolence
Sources:
100 g single, oral
Overdose
Dose: 100 g
Route: oral
Route: single
Dose: 100 g
Sources:
unhealthy, 41
Health Status: unhealthy
Age Group: 41
Sex: M
Sources:
Disc. AE: Coma...
AEs leading to
discontinuation/dose reduction:
Coma
Sources:
120 mg/kg 1 times / day multiple, intravenous
Highest studied dose
Dose: 120 mg/kg, 1 times / day
Route: intravenous
Route: multiple
Dose: 120 mg/kg, 1 times / day
Sources:
unhealthy, 62.5
Health Status: unhealthy
Age Group: 62.5
Sex: M+F
Sources:
DLT: Somnolence...
Dose limiting toxicities:
Somnolence (40%)
Sources:
60 mg/kg 1 times / day multiple, intravenous
MTD
Dose: 60 mg/kg, 1 times / day
Route: intravenous
Route: multiple
Dose: 60 mg/kg, 1 times / day
Sources:
unhealthy, 62.5
Health Status: unhealthy
Age Group: 62.5
Sex: M+F
Sources:
60 mg/kg 1 times / day multiple, oral
Recommended
Dose: 60 mg/kg, 1 times / day
Route: oral
Route: multiple
Dose: 60 mg/kg, 1 times / day
Sources:
unhealthy
Disc. AE: Hepatotoxicity, Pancreatitis...
AEs leading to
discontinuation/dose reduction:
Hepatotoxicity
Pancreatitis
Sources:
AEs

AEs

AESignificanceDosePopulation
Headache DLT
150 mg/kg single, intravenous
Highest studied dose
Dose: 150 mg/kg
Route: intravenous
Route: single
Dose: 150 mg/kg
Sources:
healthy, 30.2 ± 11.7
Health Status: healthy
Age Group: 30.2 ± 11.7
Sex: M+F
Sources:
Nausea DLT
150 mg/kg single, intravenous
Highest studied dose
Dose: 150 mg/kg
Route: intravenous
Route: single
Dose: 150 mg/kg
Sources:
healthy, 30.2 ± 11.7
Health Status: healthy
Age Group: 30.2 ± 11.7
Sex: M+F
Sources:
Somnolence Disc. AE
25 g single, oral
Overdose
Dose: 25 g
Route: oral
Route: single
Dose: 25 g
Sources:
unhealthy, 37
Health Status: unhealthy
Age Group: 37
Sex: M
Sources:
Coma Disc. AE
100 g single, oral
Overdose
Dose: 100 g
Route: oral
Route: single
Dose: 100 g
Sources:
unhealthy, 41
Health Status: unhealthy
Age Group: 41
Sex: M
Sources:
Somnolence 40%
DLT
120 mg/kg 1 times / day multiple, intravenous
Highest studied dose
Dose: 120 mg/kg, 1 times / day
Route: intravenous
Route: multiple
Dose: 120 mg/kg, 1 times / day
Sources:
unhealthy, 62.5
Health Status: unhealthy
Age Group: 62.5
Sex: M+F
Sources:
Hepatotoxicity Disc. AE
60 mg/kg 1 times / day multiple, oral
Recommended
Dose: 60 mg/kg, 1 times / day
Route: oral
Route: multiple
Dose: 60 mg/kg, 1 times / day
Sources:
unhealthy
Pancreatitis Disc. AE
60 mg/kg 1 times / day multiple, oral
Recommended
Dose: 60 mg/kg, 1 times / day
Route: oral
Route: multiple
Dose: 60 mg/kg, 1 times / day
Sources:
unhealthy
Overview

Overview

Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
minimal
minimal
minimal
no
weak [Ki 7975 uM]
weak [Ki 8553 uM]
weak [Ki 9150 uM]
yes [Ki 600 uM]
likely (co-administration study)
Comment: competitive inhibition; risk of pharmacokinetic drug–drug interactions should be taken into account during concomitant use of valproic acid and CYP2C9 substrates
Drug as victim
PubMed

PubMed

TitleDatePubMed
[Lyell syndrome associated with lamotrigine].
2000 Dec 16-31
In vivo study of the effect of valpromide and valnoctamide in the pilocarpine rat model of focal epilepsy.
2000 Nov
A case of pharmacokinetic interference in comedication of clozapine and valproic acid.
2000 Nov
Valproate-induced tinnitus misinterpreted as psychotic symptoms.
2000 Oct
[Dementia and extrapyramidal problems caused by long-term valproic acid].
2000 Sep-Oct
Action of valproic acid on Xenopus laevis development: teratogenic effects on eyes.
2001
Benzodiazepines and anticonvulsants for social phobia (social anxiety disorder).
2001
Probenecid-associated alterations in valproate glucuronide hepatobiliary disposition: mechanistic assessment using mathematical modeling.
2001 Apr
Comparison the cognitive effect of anti-epileptic drugs in seizure-free children with epilepsy before and after drug withdrawal.
2001 Apr
Determination of the antiepileptics vigabatrin and gabapentin in dosage forms and biological fluids using Hantzsch reaction.
2001 Feb
Valproate, but not lamotrigine, induces ovarian morphological changes in Wistar rats.
2001 Feb
Valproate and the risk of hyperandrogenism.
2001 Feb
Collaborative study on rat sperm motion analysis using CellSoft Series 4000 semen analyzer.
2001 Feb
Treatment and management of cluster headache.
2001 Feb
The use of baclofen in cluster headache.
2001 Feb
Distribution of valproate to subdural cerebrospinal fluid, subcutaneous extracellular fluid, and plasma in humans: a microdialysis study.
2001 Feb
Antiepileptic drug withdrawal in patients with temporal lobe epilepsy undergoing presurgical video-EEG monitoring.
2001 Feb
A case of chronic pancreatic insufficiency due to valproic acid in a child.
2001 Feb
Recommendations for the management of behavioral and psychological symptoms of dementia.
2001 Feb
[Treatment of cluster headache].
2001 Feb
Glutamate receptor antagonists differentially affect the protective activity of conventional antiepileptics against amygdala-kindled seizures in rats.
2001 Feb
Melt pelletization of a hygroscopic drug in a high shear mixer. Part 3. Effects of binder variation.
2001 Feb
Effect of coadministered drugs and ethanol on the binding of therapeutic drugs to human serum in vitro.
2001 Feb
Divalproex sodium augmentation of haloperidol in hospitalized patients with schizophrenia: clinical and economic implications.
2001 Feb
Rufinamide: a double-blind, placebo-controlled proof of principle trial in patients with epilepsy.
2001 Feb
Different control of GH secretion by gamma-amino- and gamma-hydroxy-butyric acid in 4-year abstinent alcoholics.
2001 Feb 1
Independent short-term variability of spike-like (600 Hz) and postsynaptic (N20) cerebral SEP components.
2001 Feb 12
[Maintenance dose requirement for phenytoin is lowered in genetically impaired drug metabolism independent of concommitant use of other antiepileptics].
2001 Feb 17
[Febrile convulsions, Treatment and prognosis].
2001 Feb 19
The impact of pharmacogenetics for migraine.
2001 Feb 9
Valproic acid has temporal variability in urinary clearance of metabolites.
2001 Jan
Pharmacologic treatment of patients hospitalized with the diagnosis of schizoaffective disorder.
2001 Jan
Electrophysiological and pharmacological properties of the human brain type IIA Na+ channel expressed in a stable mammalian cell line.
2001 Jan
Evaluating the tolerability of the newer mood stabilizers.
2001 Jan
Contribution of sodium valproate to the syndrome of inappropriate secretion of antidiuretic hormone.
2001 Jan
Clozapine therapy for a patient with a history of Hodgkin's disease.
2001 Jan
Effects of antiepileptic drugs on rat platelet aggregation: ex vivo and in vitro study.
2001 Jan
Occurrence of thrombocytopenia in psychiatric patients taking valproate.
2001 Jan
Additional educational needs in children born to mothers with epilepsy.
2001 Jan
Valproic acid embryopathy: report of two siblings with further expansion of the phenotypic abnormalities and a review of the literature.
2001 Jan 15
Weight change associated with valproate and lamotrigine monotherapy in patients with epilepsy.
2001 Jan 23
Hypothermia and thermoregulatory derangements induced by valproic acid.
2001 Jan 9
Reproductive effects of valproate, carbamazepine, and oxcarbazepine in men with epilepsy.
2001 Jan 9
Mood stabilizers and ion regulation.
2001 Jan-Feb
Does genomic imprinting contribute to valproic acid teratogenicity?
2001 Jan-Feb
Mood-stabilisers reduce the risk of developing antidepressant-induced maniform states in acute treatment of bipolar I depressed patients.
2001 Mar
Naltrexone as a treatment of self-injurious behavior--a case report.
2001 Mar
A phase II study to establish the efficacy and toxicity of sodium valproate in patients with cancer-related neuropathic pain.
2001 Mar
Synthesis and intramitochondrial levels of valproyl-coenzyme A metabolites.
2001 Mar 1
Placebo-controlled study of divalproex sodium for agitation in dementia.
2001 Winter
Patents

Sample Use Guides

Usual Adult Dose for Epilepsy
Route of Administration: Other
H9C2 cells were cultured and allotted to the blank, vehicle, and valproic acid (VPA)-treated groups: the VPA treated group received VPA exposure at concentrations of 2.0, 4.0 and 8.0 mmol/L. VPA might result in acetylation/deacetylation imbalances by inhibiting HDAC1-3 protein expression and total HDAC activity, leading to the down-regulation of mRNA and protein expression of Vangl2 and Scrib.
Name Type Language
VALPROATE MAGNESIUM
WHO-DD  
Systematic Name English
VALPROATE MAGNESIUM [WHO-DD]
Common Name English
MAGNESIUM DIPROPYLACETATE
Systematic Name English
MAGNESIUM VALPROATE
Systematic Name English
PENTANOIC ACID, 2-PROPYL-, MAGNESIUM SALT (2:1)
Common Name English
DIPROMAL
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
FDA ORPHAN DRUG 334411
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
NCI_THESAURUS C1946
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
Code System Code Type Description
CAS
62959-43-7
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
FDA UNII
Q400352CM2
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
PUBCHEM
147515
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
NCI_THESAURUS
C71156
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
RXCUI
134422
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY RxNorm
EVMPD
SUB05073MIG
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
ECHA (EC/EINECS)
263-770-9
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY
EPA CompTox
62959-43-7
Created by admin on Sat Jun 26 08:54:15 UTC 2021 , Edited by admin on Sat Jun 26 08:54:15 UTC 2021
PRIMARY