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Valproic acid

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Category Human immunodeficiency Virus (HIV)
CAS 99-66-1
Description Valproic acid is an inhibitor of histone deacetylase (HDAC) inhibitor, which has an anticancer effect. Valproic acid was shown to induce proliferation and enhance self-renewal of hematopoietic stem cells (HSC).
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Product Information

Synonyms VPA; 2-Propylpentanoic Acid
IUPAC Name 2-propylpentanoic acid
Molecular Weight 144.21
Molecular Formula C8H16O2
Canonical SMILES CCCC(CCC)C(=O)O
InChI InChI=1S/C8H16O2/c1-3-5-7(6-4-2)8(9)10/h7H,3-6H2,1-2H3,(H,9,10)
InChIKey NIJJYAXOARWZEE-UHFFFAOYSA-N
Boiling Point 220.0±0.0 °C at 760 mmHg
Melting Point 25 °C
Flash Point 232 °F
Purity >98%
Density 0.9±0.1 g/cm3
Solubility In vitro: 10 mM in DMSO
Appearance Colorless to light yellow (Liquid)
Application Antimanic Agents
Storage Powder: -20°C: 3 years; 4°C: 2 years In solvent: -80°C: 6 months; -20°C: 1 month
Complexity 93.4
Exact Mass 144.115029749
Index Of Refraction 1.435
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.
PSA 37.30000
Target HDAC; Autophagy; Mitophagy; HIV; Notch; Apoptosis; Endogenous Metabolite
Vapor Pressure 0.0±0.9 mmHg at 25°C
XLogP3-AA 2.8

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