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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1627 | Famotidine | MK-208 | Histamine Receptor |
Famotidine (MK-208) is a propanimidamide and histamine H2-receptor antagonist with antacid activity. As a competitive inhibitor of histamine H2-receptors located on the basolateral membrane of the parietal cell, famotidi... | |||
T68725 | Famotidine propanamide | ||
Famotidine propanamide is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. | |||
T71049 | Famotidine disulfide | ||
Famotidine disulfide is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. | |||
T71509 | Famotidine sulfamoyl propanamide | ||
Famotidine sulfamoyl propanamide is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. | |||
T71485 | Famotidine propionic acid | ||
Famotidine propionic acid is a histamine H2-receptor antagonist that inhibits stomach acid production. It is commonly used in the treatment of peptic ulcer disease and gastroesophageal reflux disease. | |||
T71470 | Famotidine hydrochloride | ||
Famotidine hydrochloride is a competitive histamine H2-receptor antagonist. Its main pharmacodynamic effect is the inhibition of gastric secretion. | |||
T71507 | PF-4522654 | ||
PF-4522654 is a potent and selective 5-HT2C receptor agonist. | |||
T71483 | Streptonigrin (racemate) | ||
Streptonigrin is an aminoquinone antitumor and antibacterial antibiotic produced by Streptomyces flocculus. Streptonigrin inhibits β-Catenin/Tcf signaling and shows cytotoxicity in β-catenin-activated cells. Streptonigri... | |||
T71047 | Annonin VI | ||
Annonin VI is a natural inhibitor of NADH:ubiquinone oxidoreductase. | |||
T71468 | Chaetochromin C | ||
Chaetochromin C also known as 4548-G05, is an orally active, small-molecule, selective agonist of the insulin receptor. |