Synthetic studies on selective type 4 phosphodiesterase (PDE 4) inhibitors. 1. Structure-activity relationships and pharmacological evaluation of 1,8-naphthyridin-2(1H)-one derivatives

Chem Pharm Bull (Tokyo). 2002 Aug;50(8):1050-9. doi: 10.1248/cpb.50.1050.

Abstract

In order to develop novel and orally active phosphodiesterase (PDE) 4 inhibitors, random screening was performed using our chemical library to find YM-10335 possessing the 1,8-naphthyridin-2(1H)-one skeleton which is a completely different structure from rolipram. In this report, the syntheses and structure-activity relationships of the YM-10335 derivatives were described. Some compounds showed selective inhibitory activities for PDE 4 derived from human peripheral blood cells and no effect on the other PDE types (1, 2, 3, 5). The inhibition of the tumor necrosis factor-alpha (TNF-alpha) release in vitro and the carrageenan-induced pleurisy in rats were also described.

MeSH terms

  • 3',5'-Cyclic-AMP Phosphodiesterases / antagonists & inhibitors*
  • 3',5'-Cyclic-AMP Phosphodiesterases / metabolism
  • Animals
  • Carrageenan / administration & dosage
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • Drug Evaluation, Preclinical / methods
  • Humans
  • Male
  • Naphthyridines / chemistry*
  • Naphthyridines / pharmacology*
  • Phosphodiesterase Inhibitors / chemistry*
  • Phosphodiesterase Inhibitors / pharmacology*
  • Pleurisy / chemically induced
  • Pleurisy / enzymology
  • Rats
  • Structure-Activity Relationship

Substances

  • Naphthyridines
  • Phosphodiesterase Inhibitors
  • Carrageenan
  • 3',5'-Cyclic-AMP Phosphodiesterases
  • Cyclic Nucleotide Phosphodiesterases, Type 4