首页 / 多肽产品 / 生物分析/药物研发 / 二肽 / Calpain Inhibitor III; Z-Val-Phe-CHO
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Calpain Inhibitor III; Z-Val-Phe-CHO
名称
Calpain Inhibitor III; Z-Val-Phe-CHO
分子结构式
CAS号
88191-84-8
分子式
C22H26O4N2
分子量
382.45
作用靶点
Proteasome
序列号
Cbz-Val-Phe-CHO
短序列号
Z-VF-CHO
国际标识符代码
NGBKFLTYGSREKK-ANYOKISRSA-N
溶解度
30 mg/mL
纯度
95%
引用文献
[1]. Chen ZF, et al. Neuronal recovery after moderate hypoxia is improved by the calpain inhibitor MDL28170. Brain Res. 1997 Sep 19;769(1):188-92. [2]. Li PA, et al. Postischemic treatment with calpain inhibitor MDL 28170 ameliorates brain damage in a gerbil model of global ischemia. Neurosci Lett. 1998 May 8;247(1):17-20. [3]. Ai J, et al. Calpain inhibitor MDL-28170 reduces the functional and structural deterioration of corpus callosum following fluid percussion injury. J Neurotrauma. 2007 Jun;24(6):960-78. [4]. De Strooper B, et al. A presenilin-1-dependent gamma-secretase-like protease mediates release of Notch intracellular domain. Nature. 1999 Apr 8;398(6727):518-22. [5]. Kharatmal SB, et al. Calpain inhibitor, MDL 28170 confer electrophysiological, nociceptive and biochemical improvement in diabetic neuropathy. Neuropharmacology. 2015 Oct;97:113-21.
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Application of the calpain inhibitor Z-VF-CHO reduced capsaicin-mediated cell death in cultured dorsal root ganglion neurons. Dong et al. observed that this inhibitor modulated Aβ formation by inhibiting the formation of intermediate Aβ 1-46 and protecting Aβ from degradation.