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Merck
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重要文件

676380

Sigma-Aldrich

Valproic Acid sodium salt

≥98% (HPLC), solid, HDAC1 inhibitor, Calbiochem®

同義詞:

丙戊酸钠盐, 2-丙基戊酸钠

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About This Item

經驗公式(希爾表示法):
C8H15NaO2
CAS號碼:
分子量::
166.19
MDL號碼:
分類程式碼代碼:
12352106
NACRES:
NA.77
暫時無法取得訂價和供貨情況

產品名稱

丙戊酸钠盐, A cell-permeable, short-chained fatty acid that inhibits histone deacetylase (IC₅₀ = 400 µM for HDAC1).

品質等級

描述

Merck USA index - 14, 9913

化驗

≥98% (HPLC)

形狀

solid

效力

400 μM IC50

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
desiccated (hygroscopic)

顏色

white

溶解度

water: 50 mg/mL

運輸包裝

ambient

儲存溫度

2-8°C

SMILES 字串

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

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 密鑰

AEQFSUDEHCCHBT-UHFFFAOYSA-M

一般說明

一种细胞可渗透性短链脂肪酸,可抑制组蛋白脱乙酰酶活性(HDAC1的IC50 = 400 µM)。诱导分化并抑制来源于人类恶性胶质瘤的细胞系的增殖。在治疗水平(350 µM-1.04 mM),引起肌醇耗竭,抑制GSK-3α和-3β,激活ERK通路,并产生神经营养效应。已被用作抗癫痫药。也有报告刺激过氧化物酶体增殖物激活受体(PPAR)活性。在人类和啮齿动物模型中显示出强效的致畸活性。

生化/生理作用

主要靶标
HDAC1
产物不与ATP竞争。
可逆:否
细胞可渗透性:是

包裝

用惰性气体包装

警告

毒性:有害 & 致癌/致畸性(E)

其他說明

Gottlicher, M., et al. 2001.EMBO J.20, 6969.
Knupfer, M.M., et al. 2001.Anticancer Res.21, 347.
Phiel, C.J., et al. 2001.J. Biol. Chem.276, 36734.
Vaden, D.L., et al. 2001.J. Biol. Chem.276, 15466.
Yuan, P.X., et al. 2001.J. Biol. Chem.276, 31674.
Chen, G., et al. 1999.J. Neurochem.72, 1327.

法律資訊

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Oral - Repr. 2

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


分析證明 (COA)

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