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Cholecystokinin Receptor

Cholecystokinin Receptor

货号 产品名 CAS号 信息
CSN26386 YM022 145084-28-2 YM022 is a highly potent, selective and orally active gastrin/cholecystokinin (CCK)-B receptor (CCK-BR) antagonist. YM022 shows the Ki values of 68 pM and 63 nM for CCK-B and CCK-A receptor, respectively[1]. YM022 can inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation in vivo[3].
CSN22510 Sograzepide 155488-25-8 Sograzepide is a gastrin/cholecystokinin 2 receptor (CCK2) antagonist.
CSN13775 2-(4-Chlorobenzamido)-3-(2-oxo-1,2-dihydroquinolin-4-yl)propanoic acid 90098-04-7 Rebamipide is an inducer of endogenous prostaglandin, an oxygen-derived free radical scavenger, and a cholecystokinin type 1 (CCK1) receptor inhibitor for inhibiting [125I]BH-CCK-8S with IC50 of 37.7 μM.
CSN23839 Proglumide 6620-60-6 Proglumide is a known cholecystokinin (CCK) antagonist.
CSN11674 Pentagastrin 5534-95-2 Pentagastrin (ICI-50123) is a selective agonist of Cholecystokinin B (CCKB) receptor with an IC50 of 11 nM. Pentagastrin is a synthetic polypeptide that has effects like gastrin when given parenterally, which can cause the secretion and synthesis of salivary proteins.
CSN18099 Nastorazepide 209219-38-5 Nastorazepide is a selective, orally available, 1,5-benzodiazepine-derivative gastrin/cholecystokinin 2 (CCK-2) receptor antagonist with potential antineoplastic activity.
CSN21716 Loxiglumide 107097-80-3 Loxiglumide is a cholecystokinin (CCK) receptor antagonist.
CSN22513 SR 146131 221671-61-0 GI 181771 is a cholecystokinin 1 receptor agonist investigated for the treatment of obesity.
CSN22411 GI 181771 305366-98-7 GI 181771 is a cholecystokinin 1 receptor agonist investigated for the treatment of obesity.
CSN21655 Gastrin I, human 10047-33-3 Gastrin I is an endogenous gastrointestinal peptide hormone that can bind to cholecystokinin (CCK) receptors.
CSN26412 Devazepide 103420-77-5 Devazepide is a potent, competitive, selective and orally active nonpeptide antagonist of cholecystokinin (CCK) receptor, with IC50s of 81 pM, 45 pM and 245 nM for rat pancreatic, bovine gallbladder and guinea pig brain CCK receptors, respectively. Devazepide is effective for gastrointestinal disorders[1].
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