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Merck
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208722

Sigma-Aldrich

钙蛋白酶抑制剂 III

The Calpain Inhibitor III, also referenced under CAS 88191-84-8, controls the biological activity of Calpain. This small molecule/inhibitor is primarily used for Protease Inhibitors applications.

别名:

钙蛋白酶抑制剂 III, 苄氧羰基-缬氨酸-苯丙氨酸,MDL 28170

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About This Item

经验公式(希尔记法):
C22H26N2O4
CAS号:
分子量:
382.45
MDL號碼:
分類程式碼代碼:
12352200
NACRES:
NA.77

品質等級

化驗

≥95% (HPLC)

形狀

lyophilized solid

效力

8 nM IC50

製造商/商標名

Calbiochem®

儲存條件

OK to freeze

顏色

white

溶解度

DMSO: 20 mg/mL (Use only anhydrous DMSO.)

運輸包裝

ambient

儲存溫度

2-8°C

InChI

1S/C22H26N2O4/c1-16(2)20(24-22(27)28-15-18-11-7-4-8-12-18)21(26)23-19(14-25)13-17-9-5-3-6-10-17/h3-12,14,16,19-20H,13,15H2,1-2H3,(H,23,26)(H,24,27)/t19-,20-/m0/s1

InChI 密鑰

NGBKFLTYGSREKK-PMACEKPBSA-N

一般說明

一种有效的细胞渗透性钙蛋白酶I和II抑制剂(Ki = 8 nM)。减少培养的背根神经节中辣椒素介导的细胞死亡。据报道,它可以阻止A23187诱导的离体海马锥体神经元神经突生长的抑制。对谷氨酸诱导的毒性表现出神经保护作用。
一种有效的细胞渗透性钙蛋白酶I和II抑制剂(Ki = 8 nM),还可减少培养的背根神经节中辣椒素介导的细胞死亡。据报道,它可以阻止A23187诱导的离体海马锥体神经元神经突生长的抑制。对谷氨酸诱导的毒性表现出神经保护作用。

生化/生理作用

主要靶标
钙蛋白酶1,钙蛋白酶2
产物不与ATP竞争。
可逆:否
细胞可渗透性:是

警告

毒性:标准处理(A)

序列

Z-Val-Phe-CHO

重構

复溶后,等分并冷冻保存(-20°C)。储备液可在-20°C最长稳定1个月。

其他說明

Chatterjee, S., et al. 1998.J. Med. Chem.41, 2663.
Rami, A., et al. 1997.Neurosci. Res. 27, 93.
Yamazaki, T., et al. 1997.Biochemistry36, 8377.
Klafki, H., et al. 1996.J. Biol. Chem.271, 28655.
Chard, P.S., et al. 1995.Neuroscience 65, 1099.
Song, D.K., et al. 1994.J. Neurosci. Res. 39, 474.

法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Vimala Bondada et al.
Biochimica et biophysica acta. Molecular cell research, 1868(7), 119019-119019 (2021-04-04)
The enzymatic characteristics of the ubiquitous calpain 5 (CAPN5) remain undescribed despite its high expression in the central nervous system and links to eye development and disease. CAPN5 contains the typical protease core domains but lacks the C terminal penta-EF

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