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Merck
CN

219385

Sigma-Aldrich

Cathepsin B Inhibitor II

≥95% (HPLC), cathepsin B inhibitor , solid

别名:

Cathepsin B Inhibitor II, Ac-LVK-CHO

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关于此项目

经验公式(希尔记法):
C19H36N4O4
分子量:
384.51
UNSPSC代码:
12352200
NACRES:
NA.77
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产品名称

Cathepsin B Inhibitor II, The Cathepsin B Inhibitor II controls the biological activity of Cathepsin B. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

质量水平

方案

≥95% (HPLC)

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze

颜色

white

溶解性

water: 1 mg/mL

运输

ambient

储存温度

−70°C

一般描述

A more active lysinal analog of Leupeptin (Cat. No. 108975). A more potent inhibitor of cathepsin B (IC50 = 4 nM) compared to leupeptin (IC50 = 310 nM).
Lysinal analog of Leupeptin (Cat. No. 108975). A more potent inhibitor of cathepsin B (IC50 = 4 nM) than of leupeptin (IC50 = 310 nM). Note: this peptide forms cyclic isomers.
Note: this peptide forms cyclic isomers.

生化/生理作用

Cell permeable: no
Primary Target
cathepsin B
Product does not compete with ATP.
Reversible: no
Target IC50: 4 nM against cathepsin B

制备说明

Following reconstitution aliquot and freeze (-70°C). Stock solutions are stable for up to 1 month at -70°C.

其他说明

Ac-Leu-Val-lysinal
McConnell, R.M., et al. 1993. J. Med. Chem. 36, 1084.

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 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Gustavo Monteiro Viana et al.
International journal of molecular sciences, 21(4) (2020-02-26)
Mucopolysaccharidosis type I (MPS I) is caused by genetic deficiency of α-l-iduronidase and impairment of lysosomal catabolism of heparan sulfate and dermatan sulfate. In the brain, these substrates accumulate in the lysosomes of neurons and glial cells, leading to neuroinflammation

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