Antiallergy agents. 1. Substituted 1,8-naphthyridin-2(1H)-ones as inhibitors of SRS-A release

J Med Chem. 1988 Nov;31(11):2108-21. doi: 10.1021/jm00119a010.

Abstract

A novel class of antiallergy agents, the substituted 1,8-naphthyridin-2(1H)-ones, is described. The present compounds are orally active, potent inhibitors of allergic and nonallergic bronchospasm in animal models. Structure-activity studies of the lead compound in this series, 1-phenyl-3-n-butyl-4-hydroxynaphthyridin-2(1H)-one (11), identified three compounds of interest, 1-phenyl-3-(2-propenyl)-4-acetoxy-1,8-naphthyridin-2(1H)-one (12), 1-(3'-chlorophenyl)-3-(2-propenyl)-4-acetoxy-1,8-naphthyridin-2(1H )-one (87), and 1-(3'-methoxyphenyl)-3-(2-propenyl)-4-acetoxy-1,8-naphthyridin-2(1 H)-one (89). The mechanism of antiallergy activity may involve inhibition of the release of the sulfidopeptide leukotrienes. 1-Phenyl-3-(2-propenyl)-4-acetoxy-1,8-naphthyridin-2(1H)-one, Sch 33303 (12), was selected for preclinical development as an antiallergy agent.

MeSH terms

  • Animals
  • Asthma / metabolism
  • Asthma / physiopathology
  • Guinea Pigs
  • Histamine H1 Antagonists / pharmacology*
  • Lung / metabolism
  • Naphthyridines / pharmacology*
  • SRS-A / metabolism*
  • Structure-Activity Relationship

Substances

  • Histamine H1 Antagonists
  • Naphthyridines
  • SRS-A
  • Sch 33303