Literature DB >> 2579236

1,2,4-Triazolo[4,3-a]quinoxaline-1,4-diones as antiallergic agents.

B Loev, J H Musser, R E Brown, H Jones, R Kahen, F C Huang, A Khandwala, P Sonnino-Goldman, M J Leibowitz.   

Abstract

A series of new 1,4-dihydro-1,2,4-triazolo[4,3-]quinoxaline-1,4-diones has been prepared. These compounds were tested as inhibitors of antigen-induced release of histamine (AIR) in vitro from rat peritoneal mast cells (RMC) and as inhibitors of IgE-mediated rat passive cutaneous anaphylaxis (PCA). Most of this new class of antiallergic agents showed good activity in the RMC and PCA tests. The most potent compound, 2-acetyl-7-chloro-5-n-propyl-1,2,4-triazolo[4,3-a]quinoxaline-1,4-dione (1x), with an I50 value of 0.1 microM, is 30 times more potent than disodium cromoglycate (DSCG) in the RMC assay.

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Year:  1985        PMID: 2579236     DOI: 10.1021/jm00381a016

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


  2 in total

1.  Synthesis and molecular structure of 6-amino-3-benzylmercapto-1,2,4-triazolo[3,4-f][1,2,4]triazin-8(7H)-one.

Authors:  Long-Chih Hwang; Chun-Hsie Tu; Jung-Hui Wang; Gene-Hsiang Lee
Journal:  Molecules       Date:  2006-03-17       Impact factor: 4.411

2.  Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4]triazolo[4,3-a]pyrimidin-7(1H)-ones.

Authors:  Awad I Said; Márta Palkó; Matti Haukka; Ferenc Fülöp
Journal:  RSC Adv       Date:  2020-09-14       Impact factor: 4.036

  2 in total

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