Synthesis and evaluation of gastroprotective and antiulcer activity of some 2-substituted-1H-imidazo[4,5-b] pyridines and -1H-benzimidazoles

Farmaco. 1992 Mar;47(3):287-303.

Abstract

Several compounds possessing imidazo[4,5-b]pyridine and benzimidazole structure bearing substituents in position 2 were prepared in order to evaluate an anti-ulcer and gastroprotective activity in rat pylorus ligature, in comparison with omeprazole. Among sixteen compounds taken as representatives of the synthetised series only one (3d) showed a good activity by i.m. administration at 50 mg/kg, while by oral administration of 100 mg/kg a certain number was active and in some cases this activity was quite superior to that of omeprazole.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Ulcer Agents / chemical synthesis*
  • Anti-Ulcer Agents / pharmacology
  • Benzimidazoles / chemical synthesis*
  • Benzimidazoles / pharmacology
  • Chemical Phenomena
  • Chemistry
  • Dogs
  • Imidazoles / chemical synthesis*
  • Imidazoles / pharmacology
  • Male
  • Omeprazole / pharmacology
  • Pylorus / physiology
  • Pyridines / chemical synthesis*
  • Pyridines / pharmacology
  • Rats
  • Rats, Inbred Strains
  • Stomach / drug effects*

Substances

  • Anti-Ulcer Agents
  • Benzimidazoles
  • Imidazoles
  • Pyridines
  • Omeprazole