Studies on antiulcer drugs. VI. 4-Furyl-2-guanidinothiazoles and related compounds as potent histamine H2-receptor antagonists

Chem Pharm Bull (Tokyo). 1992 Sep;40(9):2432-41. doi: 10.1248/cpb.40.2432.

Abstract

A series of 4-furyl-2-guanidinothiazole derivatives and related compounds were synthesized and evaluated for histamine H2-receptor antagonist and gastric acid antisecretory activities. Among them, compounds I-17, I-48 and I-49 showed high activities in these tests. In addition, compound I-17 possessed potent inhibitory activities on each of the gastric ulcers induced by stress, ethanol and HCl-aspirin. On the other hand, compound I-48 demonstrated antimicrobial activity against Helicobacter Pylori and the potency was far stronger than that of clinically used H2-antagonists. Some structure-activity relationships are discussed.

MeSH terms

  • Animals
  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / pharmacology
  • Anti-Ulcer Agents / chemical synthesis*
  • Anti-Ulcer Agents / pharmacology
  • Bacteria / drug effects
  • Dogs
  • Guanidines / chemical synthesis*
  • Guanidines / pharmacology
  • Guinea Pigs
  • Histamine H2 Antagonists / chemical synthesis*
  • Histamine H2 Antagonists / pharmacology
  • Male
  • Rats
  • Thiazoles / chemical synthesis*
  • Thiazoles / pharmacology

Substances

  • Anti-Bacterial Agents
  • Anti-Ulcer Agents
  • Guanidines
  • Histamine H2 Antagonists
  • Thiazoles