Synthesis and pharmacological profile of 1-aryl-3-substituted pyrrolo[3,2-c]quinolines

Bioorg Med Chem Lett. 1999 Oct 4;9(19):2819-22. doi: 10.1016/s0960-894x(99)00496-5.

Abstract

A series of 1-aryl-3-substituted pyrrolo[3,2-c]quinolines were synthesized and evaluated for their anti-ulcer activity. While 3-substituents of pyrrolo[3,2-c]quinolines mostly affected the in vitro H+/K+ ATPase activity, 1-aryl substituents of pyrrolo[3,2-c]quinolines affected the in vivo gastric acid secretion. In addition, the compounds with good in vivo activity protected from ethanol-induced ulcer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Ulcer Agents / chemical synthesis*
  • Anti-Ulcer Agents / pharmacology
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / pharmacology
  • Ethanol / toxicity
  • Gastric Acid / metabolism
  • Molecular Structure
  • Proton Pump Inhibitors
  • Quinolines / chemical synthesis*
  • Quinolines / pharmacology
  • Rats
  • Stomach Ulcer / chemically induced
  • Stomach Ulcer / prevention & control

Substances

  • Anti-Ulcer Agents
  • Enzyme Inhibitors
  • Proton Pump Inhibitors
  • Quinolines
  • Ethanol