Literature DB >> 1469690

Structure-activity relationships of imidazo[4,5-f]quinoline partial structures and analogs. Discovery of pyrazolo[3,4-f]quinoline derivatives as potent immunostimulants.

M P Moyer1, F H Weber, J L Gross.   

Abstract

Structure-activity studies have been carried out on a series of imidazo[4,5-f]quinoline derivatives reported to have potent in vivo immunostimulatory activity. This activity has been confirmed, and subtle structure-activity relationships have been uncovered which resulted in the identification of novel analogs (pyrazolo[3,4-f]quinoline derivatives, 7a,b) with potent in vivo effects in a mouse protection model. Regioisomeric pyrazolo[4,3-f]quinoline derivatives (6a,b) were shown to be inactive. Data are presented which support the notion that the in vivo activity is mediated by an immunostimulatory mechanism.

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Year:  1992        PMID: 1469690     DOI: 10.1021/jm00102a013

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


  3 in total

1.  Direct one-pot synthesis of primary 4-amino-2,3-diaryl-quinolines via Suzuki-Miyaura cross-coupling of 2-aryl-4-azido-3-iodoquinolines with arylboronic acids.

Authors:  Malose Jack Mphahlele; Mamasegare Mabel Mphahlele
Journal:  Molecules       Date:  2011-10-25       Impact factor: 4.411

2.  Design, synthesis and antiproliferative activity of novel 2-substituted-4-amino-6-halogenquinolines.

Authors:  Nan Jiang; Xin Zhai; Ting Li; Difa Liu; Tingting Zhang; Bin Wang; Ping Gong
Journal:  Molecules       Date:  2012-05-16       Impact factor: 4.411

3.  An efficient access to the synthesis of novel 12-phenylbenzo[6,7]oxepino[3,4-b]quinolin-13(6H)-one derivatives.

Authors:  Wentao Gao; Guihai Lin; Yang Li; Xiyue Tao; Rui Liu; Lianjie Sun
Journal:  Beilstein J Org Chem       Date:  2012-10-30       Impact factor: 2.883

  3 in total

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