Literature DB >> 16161350

Synthesis and cytotoxicity of new potential intercalators based on tricyclic systems of some pyrimido[5,4-c]cinnoline and pyrimido[5,4-c]quinoline derivatives. Part I.

Wiesława Lewgowd1, Andrzej Stańczak, Zbigniew Ochocki, Urszula Krajewska, Marek Rózalski.   

Abstract

Pyrimido[5,4-c]cinnoline and pyrimido[5,4-c]quinoline derivatives have been tested as potential intercalators. All of them embody stuctural properties alike to afford intercalating activity. Their cytotoxicity was determined on the two human leukemia cell lines, the promyelocytic HL-60 and the lymphoblastic NALM-6. The viability of cells exposed continuously to tested compounds was estimated by the trypan-blue exclusion assay. IC50 data for the NALM-6 cell line are lower than for the HL-60 cell line, what suggested that the HL-60 leukemia cells are more resistant to toxic action of tested compounds. All compounds exerted moderate cytotoxic activity. The compounds were analyzed with the HyperChem/ChemPlus software trying to find basic structure-activity relationships.

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Year:  2005        PMID: 16161350

Source DB:  PubMed          Journal:  Acta Pol Pharm        ISSN: 0001-6837            Impact factor:   0.330


  1 in total

1.  1,2,3,6,7,8-Hexahydro-cinnolino[5,4,3-cde]cinnoline.

Authors:  Zhi-Qiang Gao
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-01-08
  1 in total

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