Others Products Targets

Products for Others - Page 24

  1. Cat.No. Product Name Information/Activity
  2. BCC7319 Devazepide Devazepide (L-364,718) 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 (L-364,718) is effective for gastrointestinal disorders. Devazepide chemical structure
  3. BCC7277 SR 27897 Lintitript (SR 27897) is a highly potent, selective, orally active, competitive and non-peptide cholecystokinin (CCK1) receptor antagonist with an EC50 of 6 nM and a Ki of 0.2 nM. Lintitript displays > 33-fold selectivity more selective for CCK1 than CCK2 receptors (EC50 value of 200 nM). Lintitript increases plasma concentration of leptin and food intake as well as plasma concentration of insulin. SR 27897 chemical structure
  4. BCC5958 Gastrin I (human) Gastrin-1, human is the endogenous peptide produced in the stomach, and increases gastric acid secretion via cholecystokinin 2 (CCK2) receptor. Gastrin I (human) chemical structure
  5. BCC7430 CI 988 130332-27-3 CI 988 chemical structure
  6. BCC7477 L-365,260 118101-09-0 L-365,260 chemical structure
  7. BCC6891 LY 225910 133040-77-4 LY 225910 chemical structure
  8. BCC5772 LY 288513 147523-65-7 LY 288513 chemical structure
  9. BCC7431 PD 135158 130285-87-9 PD 135158 chemical structure
  10. BCC7052 YM 022 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. YM022 can inhibit gastrin-induced gastric acid secretion and histidine decarboxylase activation in vivo. YM 022 chemical structure
  11. BCC7480 Antalarmin hydrochloride 220953-69-5 Antalarmin hydrochloride chemical structure

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