Date published: 2026-5-25

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rac 5-Hydroxy Valproic Acid-d7 Sodium Salt

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Application:
rac 5-Hydroxy Valproic Acid-d7 Sodium Salt is a 2H-labelled metabolite of Valproic Acid
Molecular Weight:
189.24
Molecular Formula:
C8H8D7NaO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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rac 5-Hydroxy Valproic Acid-d7 Sodium Salt is a deuterium-labelled metabolite of Valproic Acid. The unlabelled version of this compound, rac 5-Hydroxy Valproic Acid (sc-208266) has been reported to be the product of the metabolism of Valproic Acid via CYP4B1, as demonstrated using monospecific polyclonal antibodies directed against CYP4B1. Valproic Acid, the parent compound of the labelled metabolite, is a branched chain, fatty acid which is reported to potentially enhance central GABAergic neurotransmission and inhibit Na+ channels. Currently, the various molecular mechanisms of action of Valproic Acid have not been completely elucidated. Valproic Acid has been reported to be a potent inhibitor of histone deacetylases (HDACs) in vitro. Valproic Acid is also noted to relieve HDAC-dependent transcriptional repression and causes the hyperacetylation of histones in cultured cells. In animal studies, Valproic Acid has been observed to reduce tumor growth and metastasis formation. Additionally, Valproic Acid is reported to activate Wnt-dependent gene expression and to mimic trichostatin A (sc-3511) in the inhibition of histone deacetylase.

Metabolites of Valproic Acid are also available as:
Valproic Acid (sc-213144)
Valproic Acid, Sodium Salt (sc-202378)
3-Hydroxy Valproic Acid (sc-209599)
3-Keto Valproic Acid Sodium Salt (sc-216476)
4-Hydroxy Valproic Acid Sodium Salt(Mixture of Diastereomers) (sc-216870)
rac 5-Hydroxy Valproic Acid Sodium Salt (sc-208266)
Valproic Acid β-D-Glucuronide Allyl Ester (sc-220360)
Valproic Acid &beat;-D-Glucuronide (sc-213145)

Labelled forms of Valproic Acid are available as:
Valproic Acid-d6 (sc-213146)
Valproic Acid-d6 β-D-Glucuronide (sc-220361)


rac 5-Hydroxy Valproic Acid-d7 Sodium Salt References

  1. Do structural properties explain the anticonvulsant activity of valproate metabolites? A QSAR analysis.  |  Bello-Ramírez, AM., et al. 2002. Epilepsia. 43: 475-81. PMID: 12027907
  2. Studies on the beta-oxidation of valproic acid in rat liver mitochondrial preparations.  |  Bjorge, SM. and Baillie, TA. 1991. Drug Metab Dispos. 19: 823-9. PMID: 1680661
  3. Development of human liver UDP-glucuronosyltransferases.  |  Burchell, B., et al. 1989. Dev Pharmacol Ther. 13: 70-7. PMID: 2515047
  4. Successful LC-MS/MS assay development and validation for determination of valproic acid and its metabolites supporting proactive pharmacovigilance.  |  Wang, WJ., et al. 2023. J Pharm Biomed Anal. 234: 115538. PMID: 37354631
  5. CYP4 isozyme specificity and the relationship between omega-hydroxylation and terminal desaturation of valproic acid.  |  Rettie, AE., et al. 1995. Biochemistry. 34: 7889-95. PMID: 7794900

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

rac 5-Hydroxy Valproic Acid-d7 Sodium Salt, 1 mg

sc-219789
1 mg
$360.00