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Merck
CN
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文件

安全信息

5.08318

Sigma-Aldrich

SHIP2 Inhibitor II, CPDA

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别名:
SHIP2 Inhibitor II, CPDA
经验公式(希尔记法):
C20H15ClF2N2O2
分子量:
388.80
UNSPSC代码:
12352200
NACRES:
NA.77

检测方案

≥98% (HPLC)

质量水平

形式

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
protect from light

颜色

white

溶解性

DMSO: 100 mg/mL

储存温度

2-8°C

一般描述

A cell-permeable aminopyridine acetamide based compound that acts as an inhibitor of SH2 domain-containing inositol 5′-phosphatase 2 (SHIP2) that can overcome insulin resistance in 3T3-L1 adipocytes. Enhances insulin-stimulated Akt phosphorylation (Thr308) in TNFa-treated 3T3-L1 adipocytes (~10 µM) and in primary cultured neurons from rat cerebral cortex. Improves glucose tolerance in db/db mice (~300 mg/kg b.i.d) without affecting their fasting glucose levels. Also reduces the expression levels of glucose-6-phosphatase and phosphoenolpyruvate carboxykinase.

生化/生理作用

Cell permeable: yes
Primary Target
SHIP2

包装

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 3 months at -20°C.

其他说明

Ichihara, Y., et al, 2013. Eur. J. Med. Chem.62, 649.

法律信息

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

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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