Synthesis and cytotoxic and analgesic activities of some 1, 5-diaryl-3-ethoxycarbonylpyrrole derivatives

J Enzyme Inhib Med Chem. 2006 Feb;21(1):113-8. doi: 10.1080/14756360500472845.

Abstract

Some 1,5-diaryl-3-ethoxycarbonyl-2-methylpyrrole derivatives were obtained by reacting 1-aryl-3-ethoxycarbonylpent-1,4-diones and a suitable aniline derivative or sulfanilamide under Paal-Knorr pyrrole synthesis conditions. The cytotoxicity of the compounds was tested and all compounds, except for compound 2 h, showed a time-dependent increase in cytotoxic activity. Analgesic activities of the compounds were determined by using the tail-flick and tail-immersion methods; some of the compounds showed potent analgesic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics* / chemical synthesis
  • Analgesics* / chemistry
  • Analgesics* / pharmacology
  • Animals
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / drug effects
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Male
  • Mice
  • Pyrroles* / chemical synthesis
  • Pyrroles* / chemistry
  • Pyrroles* / pharmacology
  • Rats
  • Tail / drug effects*

Substances

  • Analgesics
  • Pyrroles