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Merck
CN
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文件

安全信息

SCP0076

Sigma-Aldrich

Caspase 2 Inhibitor (ICH-1)

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经验公式(希尔记法):
C23H37N5O10
分子量:
543.57
UNSPSC代码:
12352200
NACRES:
NA.32

检测方案

≥95% (HPLC)

形式

lyophilized

组成

Peptide Content, ≥80%

储存条件

protect from light

储存温度

−20°C

Amino Acid Sequence

Ac-Val-Asp-Val-Ala-Asp-al

应用

Caspase 2 Inhibitor (Ac-VDVAD-CHO) is a non-selective (also inhibits caspase 3) but powerful inhibitor of caspase 2 used to study the role of caspase 2 in cell processes.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

常规特殊物品

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Michel C Maillard et al.
Bioorganic & medicinal chemistry, 19(19), 5833-5851 (2011-09-10)
Several caspases have been implicated in the pathogenesis of Huntington's disease (HD); however, existing caspase inhibitors lack the selectivity required to investigate the specific involvement of individual caspases in the neuronal cell death associated with HD. In order to explore
Bin Fang et al.
Journal of molecular biology, 360(3), 654-666 (2006-06-20)
The molecular basis for the substrate specificity of human caspase-3 has been investigated using peptide analog inhibitors and substrates that vary at the P2, P3, and P5 positions. Crystal structures were determined of caspase-3 complexes with the substrate analogs at
Ju Youn Kim et al.
Cell, 175(1), 133-145 (2018-09-18)
Nonalcoholic fatty liver disease (NAFLD) progresses to nonalcoholic steatohepatitis (NASH) in response to elevated endoplasmic reticulum (ER) stress. Whereas the onset of simple steatosis requires elevated de novo lipogenesis, progression to NASH is triggered by accumulation of hepatocyte-free cholesterol. We

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