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Chemical structure of Divalproex Sodium

GC15212

Divalproex Sodium

Also known as sodium;hydron;bis(2-propylpentanoate)

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

ChemicalCAS76584-70-8MW310.41FormulaC8H16O2·C8H15O2·Na
CAS number
76584-70-8
Molecular weight
310.41
Formula
C8H16O2·C8H15O2·Na
Solubility
≥ 14·2mg/mL in DMSO
InChIKey
MSRILKIQRXUYCT-UHFFFAOYSA-M
Catalogue number
GC15212
Brand
GLPBIO
Computed properties PubChem CID 22227467 · TPSA 80.3 Ų · H-bond donors 1 · H-bond acceptors 4
TPSA
80.3 Ų
H-bond donors
1
H-bond acceptors
4
Rotatable bonds
8
Heavy atoms
21

SMILES [H+].CCCC(CCC)C(=O)[O-].CCCC(CCC)C(=O)[O-].[Na+]

Computed descriptors from PubChem (CID 22227467), public domain. Identity cross-checked against the supplier's molecular formula and weight — verify before use.

Ordering in Israel

Lead time
Ships from the manufacturer to your lab in 8–14 business days; customs and cold chain handled by LABO Scientific.
Pricing
Quoted in ILS, excl. VAT. Add the item to your quote and we confirm the final price, usually the same business day.
Documents
Lot certificate of analysis and manufacturer SDS are emailed with your order confirmation.
Who we serve
Universities, hospitals and biotech companies across Israel. Research use only — not for diagnostic or therapeutic use.