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Merck
CN

5.34034

Sigma-Aldrich

Heterochromatin Inhibitor, HMS-I1

别名:

Heterochromatin Inhibitor, HMS-I1, 2-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)-6-methylimidazo[1,2-a]pyridine, 2-(2,3-Dihydro-1,4-benzo[b][1,4]dioxin-6-yl)-6-methylimidazo[1,2-a]pyridine, Heterochromatin Mediated Silencing Inhibitor 1

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关于此项目

经验公式(希尔记法):
C16H14N2O2
化学文摘社编号:
分子量:
266.29
UNSPSC代码:
12352200
PubChem化学物质编号:
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方案

≥98% (HPLC)

质量水平

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

pale yellow

溶解性

DMSO: 50 mg/mL

储存温度

2-8°C

SMILES字符串

CC1=CN2C=C(N=C2C=C1)C3=CC4=C(C=C3)OCCO4

一般描述

A cell-permeable imidazopyridine based compound that lacks canonical zinc chelating moieties and acts in a reversible manner to disrupt heterochromatin-mediated transcriptional gene silencing in mammalian, fungal, and plant cells (5 - 10 µM). Targets Clr3-containing Snf2/HDAC repressor complex (SHREC) and inhibits HDAC6 and HDAC10 activities. Increases G418 resistance of cen1-kanMX cells. Shown to diminish H3K9 methylation and increase H3K9 and H3K14 acetylation in cells grown in the presence of G418. Murine erythroleukemia (MEL) cells grown in the presence of this compound can overcome α-satellite repeats-mediated gene silencing.

生化/生理作用

Cell permeable: yes
Primary Target
Clr3-containing Snf2/HDAC repressor complex (SHREC)
Reversible: yes

包装

Packaged under inert gas

制备说明

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他说明

Castonguay, E., et al. 2015. Mol. Cell. Biol.35, 662.

法律信息

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

免责声明

Toxicity: Standard Handling (A)

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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