您好!欢迎来到     ChemDig
发布供应信息 我的ChemDig 供应商中心 网站导航 中文图标 中文 图标
热搜 : 阿维菌素
首页 > 产品详情 >
产品图片

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

包装
纯度
发货地 品牌 Sigma
最小起订 1
立即询价
查看联系方式
实时库存
Histone Deacetylase Inhibitor VII, 106 - CAS 937039-45-7 - Calbiochem

产品详情

中文名称 Histone Deacetylase Inhibitor VII, 106 - CAS 937039-45-7 - Calbiochem 别名
CasNo 937039-45-7 产品类别
产品编号382173
品牌Sigma
运输ambient
形式solid
警告Toxicity: Standard Handling (A)
颜色white
测定≥95% (HPLC)
分子量339.43
溶解性DMSO: 10?mg/mL
ethanol: 2.5?mg/mL
储存温度?20°C
质量水平100
储存条件OK to freeze
protect from light
MDL编号MFCD17010287

别名

Histone Deacetylase Inhibitor VII, 106 - CAS 937039-45-7 - Calbiochem,N¹-(2-Aminophenyl)-N⁷- p-tolylheptanediamide, Pimelic Diphenylamide 106

一般描述

A cell-permeable p-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 μM with 15, 30, and 180 min preincubation, respectively), while exhibiting much lower acitivity against class I HDAC8 (IC50 ≥ 5μM with 3 h preincubation) and no activity against class II HDAC4/5/7 even at concentrations as high as 180μM. Although the mode of inhibition is mechanistically competitive and reversible, due to the slow- and tight-binding nature, long preincubation is often required for effective in vitro enzyme 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 μM, respectively, in GM15850 killing). A cell-permeable p-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 μM with 15/30/180 min preincubation), while exhibiting much lower acitivity against class I HDAC8 (IC50 ≥ 5μM with 3 h preincubation) and no activity against class II HDAC4/5/7 even at concentrations as high as 180μM. Although the mode of inhibition is mechanistically competitive and reversible, due to the slow- and tight-binding nature, long preincubation is often required for effective in vitro enzyme 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 μM, respectively, in GM15850 killing).

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.

免责声明:以上所展示的信息由企业自行提供,内容的真实性 、准确性和合法性由发布企业负责,chemdig对此不承担任何保证责任。 同时我们郑重提醒各位买/卖家,
交易前 请详细核实对方身份,切勿随意打款或发货,谨防上当受骗。如发现虚假信息,请向chemdig举报。
sigmaaldrich
X

sigmaaldrich

邮箱 orderCN@merckgroup.com
联系电话 800-8193336

咨询请告知是在ChemDig上看到的,有助于交易达成。

联系电话:
Copyright © 京ICP备2023001500号