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Pentagastrin

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Chemical Structure| 5534-95-2 同义名 : "ICI-50123;AY 6608;Petogasrin;Peptavlon;Pentagastrinum;
CAS号 : 5534-95-2
货号 : A459112
分子式 : C37H49N7O9S
纯度 : 99%+
分子量 : 767.891
MDL号 : MFCD00076515
存储条件:

粉末 Keep in dark place,Sealed in dry,Store in freezer, under -20°C

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 35 mg/mL(45.58 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方:
生物活性
描述 Pentagastrin (ICI-50123) is identified as a potent, selective antagonist of the Cholecystokinin B (CCKB) receptor, with IC50 values of 11 nM for CCKB and 1100 nM for CCKA receptors. It plays a significant role in enhancing gastric mucosal defense mechanisms against acid and provides protection to the gastric mucosa from experimental damage[1].[2].
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01699113 Hypergastrinaemia Phase 1 Completed - United Kingdom ... 展开 >> Hammersmith Medicines Research London, United Kingdom 收起 <<
NCT00625495 Gastroesophageal Reflux Diseas... 展开 >>e 收起 << Phase 4 Completed - -
NCT00001229 - Completed - United States, Maryland ... 展开 >> National Heart, Lung and Blood Institute (NHLBI) Bethesda, Maryland, United States, 20892 收起 <<
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

1.30mL

0.26mL

0.13mL

6.51mL

1.30mL

0.65mL

13.02mL

2.60mL

1.30mL

参考文献

[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.