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5-Hydroxy Valproic acid-[d7] sodium salt
Category | Human immunodeficiency Virus (HIV) |
CAS | 1189994-89-5 |
Description | 5-Hydroxy Valproic acid-[d7] sodium salt is the labelled analogue of 5-Hydroxy Valproic acid sodium salt, which is a metabolite of Valproic Acid. |
Product Information
Synonyms | 5-Hydroxy Valproic acid-d7 sodium salt; 5-OH-VPA-d7; 5-Hydroxy-2-(propyl-d7)pentanoic Acid; 2-(Propyl-d7)-5-hydroxypentanoic Acid Sodium Salt; 2-N-(Propyl-d7)-5-hydroxypentanoic Acid Sodium Salt; rac 5-Hydroxy Valproic Acid-d7 Sodium Salt |
IUPAC Name | sodium;3,3,4,4,5,5,5-heptadeuterio-2-(3-hydroxypropyl)pentanoate |
Molecular Weight | 189.24 |
Molecular Formula | C8H8D7NaO3 |
Canonical SMILES | CCCC(CCCO)C(=O)[O-].[Na+] |
InChI | InChI=1S/C8H16O3.Na/c1-2-4-7(8(10)11)5-3-6-9;/h7,9H,2-6H2,1H3,(H,10,11);/q;+1/p-1/i1D3,2D2,4D2; |
InChIKey | CSZWWXWOLIYBAB-MDVNJVHASA-M |
Purity | ≥95%; ≥99% atom D |
Solubility | Soluble in Methanol (Slightly, Sonicated) |
Appearance | White to Pale Yellow Solid |
Storage | Store at -20°C under inert atmosphere |
In Vitro | Valproic acid (VPA) (0-15 mM; 24 and 72 h) inhibits Hela cell growth in a dose- and time- dependent manner. Valproic acid (10 mM; 24 h) significantly attenuates the activities of total, cytosol and nuclear HDACs. Valproic acid (0-15 mM; 24 h) induces a G1 phase arrest at 1-3 mM and a G2/M phase arrest at 10 mM, and increases the percentage of sub-G1 cells in HeLa cells. Valproic acid also induces necrosis, Apoptosis and Lactate dehydrogenase (LDH) release. Valproic acid (0-20 mM; 24 h) activates Tcf/Lef-dependent transcription and synergizes with lithium. Valproic acid (0-5 mM; 0-18 h) increases β-catenin levels in Neuro2A cells. Valproic acid (0-2 mM; 0-24 h) stimulates phosphorylation of AMPK and ACC in hepatocytes. Valproic acid (0-10 mM; 2 days) induces Notch1 signaling and morphologic differentiation, suppresses production of NE tumor markers in SCLC cells. |
In Vivo | Valproic acid (VPA) (500 mg/kg; i.p.; daily for 12 days) inhibits tumor angiogenesis in mice transplanted with Kasumi-1 cells. Valproic acid (350 mg/kg; i.p.; once) enhances social behavior in rats. Valproic acid (0.26% (w/v); p.o. via drinking water; 14 days) decreases liver mass, hepatic fat accumulation, and serum glucose in obese mice without hepatotoxicity. |
Target | HDAC; Autophagy; Mitophagy; HIV; Notch; Endogenous Metabolite |