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位置: 首页> 品牌> Sigma-Aldrich> Histone Deacetylase Inhibitor VII, 106-CAS 937039-45-7-Calbiochem

Histone Deacetylase Inhibitor VII, 106-CAS 937039-45-7-Calbiochem

品牌
Sigma-Aldrich
CAS
937039-45-7
货号
382173
规格纯度
The Histone Deacetylase Inhibitor VII, 106, also referenced under CAS 937039-45-7, controls the biological activity of Histone Deacetylase. This small molecule/inhibitor is primarily used for Cell Structure applications.
价格
6686.93 *本价格含增值税费
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半岛bd体育手机客户端 名称:
937039-45-7
Histone Deacetylase Inhibitor VII, 106-CAS 937039-45-7-Calbiochem
N 1-(2-Aminophenyl)-N 7- p-tolylheptanediamide, Pimelic Diphenylamide 106
半岛bd体育手机客户端 介绍:

半岛bd体育手机客户端 说明

一般描述

A cell-permeablep-tolylbenzamide and a Histone Deacetylase (HDAC) Inhibitor IV (Cat. No. 382170) analog that acts as a selective inhibitor against class I HDAC1,2,3 (IC50= 0.15, 0.76, and 0.37 ?M with 15, 30, and 180 min preincubation, respectively), while exhibiting much lower acitivity against class I HDAC8 (IC50≥ 5?M with 3 h preincubation) and no activity against class II HDAC4/5/7 even at concentrations as high as 180?M. Although the mode of inhibition is mechanistically competitive and reversible, due to the slow- and tight-binding nature, long preincubation is often required for effectivein vitroenzyme inhibition, while 106-induced cellular H3 hyperacetylation is shown to persist for more than 6 hours after inhibitor removal by washing in GM15850 culture. 106 is reported to be less cytotoxic than TSA (Cat. No. 647925), MS-275, and SAHA (EC50= 6.3, 0.328, 0.768, and 1.5 ?M, respectively, in GM15850 killing).
A cell-permeablep-tolylbenzamide and a Histone Deacetylase (HDAC) Inhibitor IV (Cat. No. 382170) analog that acts as a selective inhibitor against class I HDAC1/2/3 (IC50= 0.15/0.76/0.37 ?M with 15/30/180 min preincubation), while exhibiting much lower acitivity against class I HDAC8 (IC50≥ 5?M with 3 h preincubation) and no activity against class II HDAC4/5/7 even at concentrations as high as 180?M. Although the mode of inhibition is mechanistically competitive and reversible, due to the slow- and tight-binding nature, long preincubation is often required for effectivein vitroenzyme inhibition, while 106-induced cellular H3 hyperacetylation is shown to persist for more than 6 hours after inhibitor removal by washing in GM15850 culture. 106 is reported to be less cytotoxic than TSA (Cat. No. 647925), MS-275, and SAHA (EC50= 6.3, 0.328, 0.768, and 1.5 ?M, respectively, in GM15850 killing).

包装

5 mg in Plastic ampoule
Packaged under inert gas

警告

Toxicity: Standard Handling (A)

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.

其他说明

Chou, C.J., et al. 2008.J. Biol. Chem.283,35402.

法律信息

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

基本信息

经验(实验)分子式 C20H25N3O2
分子量 339.43
MDL编号 MFCD17010287

半岛bd体育手机客户端 性质

质量水平 100
测定 ≥95% (HPLC)
形式 solid
manufacturer/tradename Calbiochem?
储存条件 OK to freeze
protect from light
颜色 white
溶解性 DMSO: 10 mg/mL
ethanol: 2.5 mg/mL
运输 ambient
储存温度 ?20℃

安全信息

储存分类代码 11 - Combustible Solids
WGK WGK 3
闪点(F) Not applicable
闪点(C) Not applicable

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