Valproic acid (sodium) (2:1)
Valproic acid (VPA) sodium (2:1) is an orally active HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid sodium (2:1) activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium (2:1) is used in the treatment of epilepsy, bipolar disorder, metabolic disease, HIV infection and prevention of migraine headaches[1][2][3][4][5][6][7].
Product Specifications
CAS Number
[76584-70-8]
Product Name Alternative
Sodium Valproate (2:1) ; VPA (sodium) (2:1) ; 2-Propylpentanoic acid (sodium) (2:1)
UNSPSC
12352211
Hazard Statement
H228
Target
Apoptosis; Autophagy; Endogenous Metabolite; HDAC; HIV; Mitophagy; Notch
Type
Reference compound
Related Pathways
Anti-infection; Apoptosis; Autophagy; Cell Cycle/DNA Damage; Epigenetics; Metabolic Enzyme/Protease; Neuronal Signaling; Stem Cell/Wnt
Applications
Cancer-Kinase/protease
Field of Research
Cancer; Infection; Metabolic Disease; Neurological Disease
Assay Protocol
https://www.medchemexpress.com/valproic-acid-sodium-2-1.html
Solubility
10 mM in DMSO
Smiles
CCCC(CCC)C([O-])=O.[0.5Na+]
Molecular Formula
C8H15O2.1/2Na
Molecular Weight
154.71
Precautions
P210-P240-P241-P280-P370+P378
References & Citations
Shipping Conditions
Room temperature
Scientific Category
Reference compound1
Clinical Information
Launched
Isoform
HDAC; HDAC1; HDAC2
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