Nonsteroidal antiinflammatory agents, XVII: Inhibition of bovine cyclooxygenase and 5-lipoxygenase by N-alkyldiphenyl-pyrrolyl acetic and propionic acid derivatives

Arch Pharm (Weinheim). 1993 Mar;326(3):157-62. doi: 10.1002/ardp.19933260308.

Abstract

A series of 19 N-alkyl-diarylpyrrolyl-acetic and-propionic acid derivatives was synthesized and tested. Using bovine blood as enzyme source the inhibition of cyclooxygenase and 5-lipoxygenase, respectively, was applied to determine the antiinflammatory activity. In general all compounds tested inhibit 5-lipoxygenase more effectively than cyclooxygenase. A structure-activity relationship is discussed.

MeSH terms

  • Acetates / chemical synthesis*
  • Acetates / pharmacology
  • Animals
  • Blood Platelets / enzymology
  • Cattle
  • Cyclooxygenase Inhibitors / chemical synthesis*
  • Cyclooxygenase Inhibitors / pharmacology
  • In Vitro Techniques
  • Lipoxygenase Inhibitors / chemical synthesis*
  • Lipoxygenase Inhibitors / pharmacology
  • Neutrophils / enzymology
  • Propionates / chemical synthesis*
  • Propionates / pharmacology

Substances

  • Acetates
  • Cyclooxygenase Inhibitors
  • Lipoxygenase Inhibitors
  • Propionates