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Merck
CN
所有图片(1)

主要文件

566660

Sigma-Aldrich

SAG

≥98% (HPLC), solid, smoothened agonist, Calbiochem®

别名:

平滑激动剂,SAG

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About This Item

经验公式(希尔记法):
C28H28ClN3OS · 2HCl · 2H2O
分子量:
599.01
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

产品名称

平滑激动剂,SAG, A cell-permeable Smoothened Agonist, SAG, CAS 364590-63-6, modulates the coupling of Smo with its downstream effector by interacting with the Smo heptahelical domain (KD = 59 nM).

质量水平

方案

≥98% (HPLC)

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
desiccated (hygroscopic)
protect from light

颜色

light yellow

溶解性

DMSO: 10 mg/mL
water: 25 mg/mL

运输

ambient

储存温度

2-8°C

SMILES字符串

[s]1c2c(c(c1C(=O)N(C5CCC(CC5)NC)Cc3cc(ccc3)c4ccncc4)Cl)cccc2.Cl.Cl.O

InChI

1S/C28H28ClN3OS.2ClH.H2O/c1-30-22-9-11-23(12-10-22)32(28(33)27-26(29)24-7-2-3-8-25(24)34-27)18-19-5-4-6-21(17-19)20-13-15-31-16-14-20;;;/h2-8,13-17,22-23,30H,9-12,18H2,1H3;2*1H;1H2

InChI key

IYXUQUYRWPGIQL-UHFFFAOYSA-N

一般描述

一种细胞渗透性Smoothened激动剂,SAG,可通过与Smo七次跨膜螺旋结构域(KD = 59 nM)相互作用,调节Smo与其下游效应器的偶联。
一种细胞渗透性苯并噻吩化合物,可通过与Smo七次跨膜螺旋结构域(KD = 59 nM)相互作用,调节Smo与其下游效应器的偶联。显示可诱导Smo内化。显示可诱导刺猬通路激活(NIH 3T3衍生Shh-LIGHT2细胞中的EC50 ∼3 nM)并抵消环巴胺-KAAD(目录号239804)对Smo的抑制。据报道,在低浓度下作为激活剂,在极高浓度下作为抑制剂。也可提供10 mM (500 µg/86 µl)Smoothened激动剂,SAG (目录号566661)的H2O溶液。
一种细胞渗透性苯并噻吩化合物,可通过与Smo七次跨膜螺旋结构域(KD = 59 nM)相互作用,调节Smo与其下游效应器的偶联。显示可诱导Smo内化。显示可诱导刺猬通路激活(NIH 3T3衍生Shh-LIGHT2细胞中的EC50 ∼3 nM)并抵消环巴胺-KAAD(目录号239804)对Smo的抑制。据报道,在低浓度下作为激活剂,在极高浓度下作为抑制剂。

包装

用惰性气体包装

警告

毒性:标准处理(A)

重悬

复溶后,等分并冷冻保存(-20°C)。贮备溶液在-20°C下可稳定保存至多6个月。

其他说明

Wang, J., et al. 2010.Proc.Natl.Acad.Sci. USA.107, 9323.
Meloni, A.R., et al. 2006.Mol.Cell.Biol.26, 7750.
Chen, W., et al. 2004.Science306, 2257.
Chen, J.K., et al. 2002.Proc.Natl.Acad.Sci. USA99, 14071.
Frank-Kamenetsky, M., et al. 2002.J. Biol.1, 10.

法律信息

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

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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