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- 保存条件:
4°C, sealed storage, away from moisture
- 英文名:
Sodium Valproate; VPA sodium; 2-Propylpentanoic acid sodium
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
1069-66-5
- 规格:
500 mg/1 g/5 g/25 g
| 规格: | 500 mg | 产品价格: | ¥350.0 |
|---|---|---|---|
| 规格: | 1 g | 产品价格: | ¥450.0 |
| 规格: | 5 g | 产品价格: | ¥800.0 |
| 规格: | 25 g | 产品价格: | ¥1000.0 |
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Valproic acid sodium
CAS No. : 1069-66-5
MCE 国际站:Valproic acid sodium
产品活性:Valproic acid sodium salt (Sodium Valproate) 是一种 HDAC 抑制剂,IC50 值为 0.5-2 mM,抑制 HDAC1 的活性,(IC50,400 μM),同时可诱导 HDAC2 的降解。Valproic acid sodium salt 激活 Notch1 信号并抑制小细胞肺癌 (SCLC) 细胞的增殖。Valproic acid sodium salt 可用于癫痫、双相情感障碍和偏头痛等的研究。
研究领域:Cell Cycle/DNA Damage | Epigenetics | Autophagy | Anti-infection | Stem Cell/Wnt | Neuronal Signaling | Metabolic Enzyme/Protease
作用靶点:HDAC | Autophagy | Mitophagy | HIV | Notch | Endogenous Metabolite
In Vitro: Valproic acid sodium salt (Sodium Valproate) inhibits the growth dose- and time-dependently with an IC50 of appr 10 and 4 mM at 24 and 72 h, respectively. Valproic acid sodium salt significantly attenuates the activities of total, cytosol and nuclear HDACs. Valproic acid sodium salt increases the form of acetylated histone 3 in HeLa cells. Valproic acid sodium salt (1-3 mM) induces a G1 phase arrest, while 10 mM Valproic acid sodium salt significantly induces a G2/M phase arrest of cell cycle in HeLa cells. In addition, Valproic acid sodium salt increases the percentage of sub-G1 cells in HeLa cells in a dose-dependent manner at 24 h.
Valproic acid sodium salt inhibits the mRNA and protein expression of VEGF, VEGFR2 and bFGF. Valproic acid sodium salt inhibits the protein expression of HDAC1, increases histone H3 acetylation, and enhances the accumulation of hyperacetylated histone H3 on VEGF promoters.
Valproic acid sodium salt treatment results in increased levels of phosphorylated AMPK/ACC in primary mouse hepatocytes. Phosphorylation of ACC following Valproic acid sodium salt treatment is AMPK-dependent. Valproic acid sodium salt inhibits the deacetylase activity of both mouse liver nuclear extracts and human recombinant HDAC1 while of the metabolites of Valproic acid, only 2-ene-Valproic acid and 4-ene-Valproic acid diminish deacetylase activity.
In Vivo: Valproic acid sodium salt (Sodium Valproate; 500 mg/kg, i.p.) inhibits the tumor growth and angiogenesisin the mice transplanted with Kasumi-1 cells. The IR rate in the Valproic acid sodium salt group is 57.25% at the end of the experiment.
Valproic acid sodium salt (350 mg/kg, i.p.) demonstrates more social investigation and play fighting than control animals.
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文献和实验of pluripotent P19 cells into skeletal muscle lineage by using histone deacetylase inhibitor, valproic acid and the ligand of retinoic acid receptor, all-trans retinoic acid.
Generation of iPS Cells from Human Skin Biopsy
human fibroblasts from skin biopsies using retroviral transduction of OCT4, SOX2, KLF4, and c-MYC with the addition of the histone deacetylase (HDAC) inhibitor, valproic acid (VPA). Characterized patient-specific iPS cell lines can be obtained
Quantifying In Vivo Phosphoinositide Turnover in Chemotactically Competent Dictyostelium Cells
of great importance. We have shown the acute reduction of PI phosphorylation in response to a widely used bipolar disorder and epilepsy treatment, valproic acid, as a potential therapeutic role for the drug using chemotactically competent Dictyostelium
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