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pubmed-article:16161350pubmed:abstractTextPyrimido[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.lld:pubmed
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pubmed-article:16161350pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:16161350pubmed:articleTitleSynthesis 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.lld:pubmed
pubmed-article:16161350pubmed:affiliationDepartment of Pharmaceutical Chemistry and Drug Analysis, Medical University of Lód?, 1 Muszy?skiego Str., 90-151 Lód?, Poland.lld:pubmed
pubmed-article:16161350pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:16161350pubmed:publicationTypeComparative Studylld:pubmed
pubmed-article:16161350pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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