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Merck
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主要文件

537011

Sigma-Aldrich

Prolyl Endopeptidase Inhibitor II

The Prolyl Endopeptidase Inhibitor II, also referenced under CAS 108708-25-4, controls the biological activity of Prolyl Endopeptidase. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

别名:

Prolyl Endopeptidase Inhibitor II, Z-PP-CHO

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About This Item

经验公式(希尔记法):
C18H22N2O4
分子量:
330.38
分類程式碼代碼:
12352200

品質等級

化驗

≥97% (HPLC)

形狀

oil

製造商/商標名

Calbiochem®

儲存條件

OK to freeze
protect from light

顏色

colorless to off-white

溶解度

DMSO: 10 mg/mL
DMF: soluble
ethyl acetate: soluble

運輸包裝

ambient

儲存溫度

−20°C

一般說明

A cell-permeable dipeptide aldehyde that acts as a specific, potent, slow and tight-binding transition state analog inhibitor of prolyl endopeptidase (Ki = 350 pM and 500 pM for mouse brain and human brain prolyl endopeptidase, respectively). Reported to form a hemiacetal with the active-site serine.
A cell-permeable dipeptide aldehyde that acts as a specific, potent, slow, and tight-binding transition state analog inhibitor of prolyl endopeptidase (Ki = 350 pM and 500 pM for mouse brain and human brain, respectively). Reported to form a hemiacetal with the active site serine of the enzyme.

生化/生理作用

Cell permeable: yes
Primary Target
Mouse brain prolylendooeotidase
Product does not compete with ATP.
Reversible: no
Target Ki: 350 pM and 500 pM for mouse brain and human brain prolyl endopeptidase, respectively

包裝

Packaged under inert gas

警告

Toxicity: Standard Handling (A)

序列

Z-Pro-Pro-CHO

重構

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他說明

Fülöp, V., et al. 1998. Cell94, 161.
Kahyaoglu, A., et al. 1997. Biochem. J.322, 839.
Bakker, A.V., et al. 1990. Biochem. J.271, 559.
Wilk, S., and Orlowski, M. 1983. J. Neurochem.41, 69.

法律資訊

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

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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