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肿瘤抗原肽(定制)

Pentagastrin

名称
Pentagastrin
分子结构式
分子量
768.79
分子式
C37H50N7O9S1
短序列号
Boc-beta-AWMDF-NH2
序列号
Boc-beta-Ala-Trp-Met-Asp-Phe-NH2
国际标识符代码
NEYNJQRKHLUJRU-DZUOILHNSA-N
纯度
≥95%
作用靶点
Cholecystokinin Receptor
DMSO溶解度
≥ 34 mg/mL
水中溶解度
< 0.1 mg/mL
引用文献
[1]. Smith AJ, et al. Characterisation of CCKB receptors on GH3 pituitary cells: receptor activation is linked to Ca2+ mobilisation. Eur J Pharmacol. 1994 Apr 15;267(2):215-23. [2]. Tanaka S, et al. Pentagastrin gastroprotection against acid is related to H2 receptor activation but not acid secretion. Gut. 1998 Sep;43(3):334-41.
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Pentagastrin (ICI-50123) is a potent, selective Cholecystokinin B (CCKB) receptor antagonists with IC50 values of 11 nM and 1100 nM for CCKB and CCKA, respectively. Pentagastrin enhances gastric mucosal defense mechanisms against acid and protects the gastric mucosa from experimental injury.