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Pharmazie ; 59(12): 899-905, 2004 Dec.
Article in English | MEDLINE | ID: mdl-15638075

ABSTRACT

In an effort to establish new antiulcer agents a series of 2-(2-substituted amino)-1 H-benzimidazoles 8, 9, 14; 1,3-disubstituted-3,4-dihydropyrimido[1,6-a]benzimidazoles 4, 7, 11, 12; 3-substituted-3,4-dihydropyrimido[1,6-a]benzimidazol-1 (2H)-thiones (or (2H)-ones) 10, 17 and 3-substituted-1,2,3,4-tetrahydropyrimido[1,6-a]benzimidazoles 15 were synthesized. Representative members were selected to evaluate their gastric antisecretory activity using an in vivo pylorus ligated rat method. Omeprazole was used as reference. The results indicated that the test compounds exhibit gastric antisecretory activity. The percent inhibition+/-SEM at the indicated dose level was demonstrated as omeprazole (59%+/-0.16 at 3 mg/kg) > 15a (53%+/-1.39 at 3 mg/kg) > 7a (51%+/-1.04 at 1 mg/kg) > 10a (50%+/-1.36 at 3 mg/kg).


Subject(s)
Anti-Ulcer Agents/chemical synthesis , Anti-Ulcer Agents/pharmacology , Benzimidazoles/chemical synthesis , Benzimidazoles/pharmacology , Pyrimidines/chemical synthesis , Pyrimidines/pharmacology , Animals , Body Weight , Gastric Mucosa/drug effects , Gastric Mucosa/metabolism , Indicators and Reagents , Male , Omeprazole/pharmacology , Pylorus/physiology , Rats , Structure-Activity Relationship
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