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Merck
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219426

Sigma-Aldrich

Cathepsin L Inhibitor II

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

别名:

Z-FY-CHO

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About This Item

UNSPSC代码:
12352200
NACRES:
NA.77

质量水平

100

方案

≥95% (HPLC)

表单

solid

制造商/商品名称

Calbiochem®

储存条件

OK to freeze

颜色

off-white

溶解性

ethanol: 50 mg/mL
DMSO: soluble

运输

ambient

储存温度

−20°C

一般描述

A potent and selective inhibitor of Cathepsin L (Cat. No. 219402).

生化/生理作用

Cell permeable: yes
Product does not compete with ATP.
Reversible: no

包装

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

序列

Z-Phe-Tyr-CHO

其他说明

Woo, J.-T., et al. 1996. Eur. J. Pharmacol. 300, 131.

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 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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Stephan Quintin et al.
The Journal of biological chemistry, 299(7), 104912-104912 (2023-06-13)
α-synuclein (αS) is an abundant, neuronal protein that assembles into fibrillar pathological inclusions in a spectrum of neurodegenerative diseases that include Lewy body diseases (LBD) and Multiple System Atrophy (MSA). The cellular and regional distributions of pathological inclusions vary widely
Prashant Gaikwad et al.
microPublication biology, 2022 (2023-01-07)
Several studies have indicated a role for cathepsin L (CTSL) proteolytic activity in the nucleus under distinct cellular conditions, including during differentiation, senescence, and quiescence. Here we show that addition of CTSL inhibitors to a cell lysis buffer prevents the

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