Literature DB >> 2903244

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

M H Sherlock1, J J Kaminski, W C Tom, J F Lee, S C Wong, W Kreutner, R W Bryant, A T McPhail.   

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.

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Year:  1988        PMID: 2903244     DOI: 10.1021/jm00119a010

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  3 in total

1.  Synthesis of 3,4-dihydro-1,8-naphthyridin-2(1H)-ones via microwave-activated inverse electron-demand Diels-Alder reactions.

Authors:  Salah Fadel; Youssef Hajbi; Mostafa Khouili; Said Lazar; Franck Suzenet; Gérald Guillaumet
Journal:  Beilstein J Org Chem       Date:  2014-01-28       Impact factor: 2.883

2.  Design, in silico studies, and synthesis of new 1,8-naphthyridine-3-carboxylic acid analogues and evaluation of their H1R antagonism effects.

Authors:  Vinod Kumar Gurjar; Dilipkumar Pal
Journal:  RSC Adv       Date:  2020-04-06       Impact factor: 4.036

3.  An improved solvent-free synthesis of flunixin and 2-(arylamino) nicotinic acid derivatives using boric acid as catalyst.

Authors:  Mahsa Yarhosseini; Shahrzad Javanshir; Zahra Dolatkhah; Mohammad G Dekamin
Journal:  Chem Cent J       Date:  2017-12-01       Impact factor: 4.215

  3 in total

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