Divalproex Sodium
Divalproex sodium is a histone deacetylase (HDAC) inhibitor and anticonvulsant agent that elevates brain GABA levels by inhibiting its catabolism and reuptake, while also blocking voltage-sensitive sodium channels. It is widely used in neuroscience research for studying epilepsy, bipolar disorder, and neuropathic pain mechanisms in both cellular and animal models.
Product Specifications
CAS Number
76584-70-8
Product Name Alternative
Histone deacetylases, HIV, Inhibitor, hepatic fat accumulation, headaches, HDAC, Human immunodeficiency virus, GABAReceptor, GABA Receptor, Endogenous Metabolite, epilepsy, Epival, Mitochondrial Autophagy, Mitophagy, migraine, inhibit, Notch, Notch1, 2-Propylpentanoic Acid (sodium) (2:1), anticonvulsant, anticancer, Apoptosis, Autophagy, bipolar disorder, degradation, Divalproex Sodium, proteasomal, small cell lung cancer, SCLC, Valproate semisodium, Valproic acid (sodium) (2:1), VPA (sodium) (2:1)
Field of Research
Cell Biology, Epigenetics & Chromatin, Infectious Disease & Virology, Metabolism Research, Molecular Biology, Neuroscience, Pharmacology & Drug Discovery, Protein Biochemistry, Stem Cell & Developmental Biology
Purity
99.84% (May vary between batches)
Solubility
Ethanol:58 mg/mL (186.85 mM) ; H2O:57 mg/mL (183.63 mM) ; DMSO:75 mg/mL (241.62 mM)
Smiles
[Na+].CCCC (CCC) C (O) =O.CCCC (CCC) C ([O-]) =O
Molecular Formula
C8H16O2·C8H15O2·Na
Molecular Weight
310.41
Storage Conditions
-20°C
Notes
For research use only.
Available Sizes
Frequently Asked Questions
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