Literature DB >> 15084122

Synthesis, biological activity, and quantitative structure-activity relationship study of azanaphthalimide and arylnaphthalimide derivatives.

Miguel F Braña1, Ana Gradillas, Angel Gómez, Nuria Acero, Francisco Llinares, Dolores Muñoz-Mingarro, Cristina Abradelo, Fernanda Rey-Stolle, Mercedes Yuste, Joaquín Campos, Miguel A Gallo, Antonio Espinosa.   

Abstract

A series of quinoline derivatives as aza analogues of the naphthalene chromophore and a series of "nonfused" tricyclic aromatic systems, in particular 5-arylquinolines and 5- or 6-aryl and heteroaryl naphthalene systems, were synthesized and evaluated for growth-inhibitory properties in several human cell lines. The analysis of quantitative structure-antitumor activity relationships for the growth-inhibitory properties is also reported. Findings suggest that these compounds may not express their cytotoxicity via interaction on DNA.

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Year:  2004        PMID: 15084122     DOI: 10.1021/jm0310784

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


  3 in total

1.  Spectroscopic and quantum mechanical approach of solvatochromic immobilization: modulation of electronic structure and excited-state properties of 1,8-naphthalimide derivative.

Authors:  Soumya Sundar Mati; Sayantani Chall; Soumyadipta Rakshit; Subhash Chandra Bhattacharya
Journal:  J Fluoresc       Date:  2015-02-14       Impact factor: 2.217

2.  Novel naphthalimide polyamine derivatives as potential antitumor agents.

Authors:  Robert Seliga; Martina Pilatova; Marek Sarissky; Viktor Viglasky; Martin Walko; Jan Mojzis
Journal:  Mol Biol Rep       Date:  2013-05-03       Impact factor: 2.316

3.  Reductive Heck reactions of N-methyl-substituted tricyclic imides.

Authors:  Gokce Goksu; Nuket Ocal; Dieter E Kaufmann
Journal:  Molecules       Date:  2010-03-04       Impact factor: 4.411

  3 in total

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