Literature DB >> 3172129

Synthesis and antineoplastic evaluation of 1,4-bis(aminoalkanamido)-9,10-anthracenediones.

S Martelli1, M Dzieduszycka, B Stefanska, M Bontemps-Gracz, E Borowski.   

Abstract

The effect of the replacement of amino groups, attached to the anthraquinone ring in [(aminoalkyl)amino]-anthraquinones, by an amido function on DNA binding, cytotoxicity, and antileukemic activity has been studied. The corresponding 1,4-bis(aminoalkanamido)-9,10-anthracenediones have been synthesized and examined. It has been concluded that such modification does not exclude the DNA binding and cytotoxicity of mentioned compounds but decreases or abolishes the in vivo antileukemic activity.

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Year:  1988        PMID: 3172129     DOI: 10.1021/jm00118a015

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


  2 in total

Review 1.  Rationale for the use of aliphatic N-oxides of cytotoxic anthraquinones as prodrug DNA binding agents: a new class of bioreductive agent.

Authors:  L H Patterson
Journal:  Cancer Metastasis Rev       Date:  1993-06       Impact factor: 9.264

2.  A highly facile approach to the synthesis of novel 2-(3-benzyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-N-phenylacetamides.

Authors:  Mikhail S Novikov; Denis A Babkov; Maria P Paramonova; Alexander O Chizhov; Anastasia L Khandazhinskaya; Katherine L Seley-Radtke
Journal:  Tetrahedron Lett       Date:  2012-11-29       Impact factor: 2.415

  2 in total

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