Valproic Acid, Sodium Salt | 1647

A cell-permeable histone deacetylase 1 (HDAC1) inhibitor (IC₅₀ = 400 µM) that exhibits anticancer, anti-inflammatory and neuroprotective properties. Recently it has been reported that Valproic acid enables reprogramming of primary human fibroblasts with only two factors, Oct4 and Sox2, without the need for the oncogenes c-Myc or Klf4.

Valproic Acid, Sodium Salt is a cell-permeable histone deacetylase 1 (HDAC1) inhibitor (IC₅₀ = 400 µM) that exhibits anticancer, anti-inflammatory and neuroprotective properties.

1647 | Valproic Acid, Sodium Salt DataSheet

Alternate Name/Synonyms: Valproic acid sodium, Sodium Valproate, VPA

Appearance: White solid

Formulation: N/A

CAS Number: 1069-66-5

Structure Available?: Yes

Peptide sequence: N/A

Salt Form: No

Molecular Formula: C₈H₁₅O₂.Na

Molecular Weight: 166.19

Cell-Permeable?: No

Purity: ≥98% by titration

Solubilities: H₂O (100 mM)

Handling: Protect from air and moisture

Country of Origin: USA

Tag Line: A HDAC1 inhibitor

MDL Number: MFCD00078604

PubChem CID: 16760703

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

InChi: InChI=1S/C8H16O2.Na/c1-3-5-7(6-4-2)8(9)10;/h7H,3-6H2,1-2H3,(H,9,10);/q;+1/p-1

InChi Key: AEQFSUDEHCCHBT-UHFFFAOYSA-M