Abstract
Benzo[c][1,7] and [1,8]phenanthroline substituted by dialkylaminoalkyl side chains at position C2 and C1, respectively, were synthesized and their biological activity evaluated. These compounds displayed more potent cytotoxicity toward L1210 cells than the parent unsubstituted compounds, associated with strong DNA interaction. The moderate TopoI inhibitory activity induced by the novel compounds suggests that other cellular targets should be responsible for the antiproliferative activity.
Copyright (c) 2010 Elsevier Masson SAS. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Base Sequence
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Circular Dichroism
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DNA / chemistry
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DNA / genetics
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DNA / metabolism
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Humans
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Mice
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Molecular Sequence Data
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Nucleic Acid Denaturation
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Phenanthrolines / chemical synthesis*
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Phenanthrolines / chemistry
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Phenanthrolines / metabolism
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Phenanthrolines / pharmacology*
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Spectrophotometry, Ultraviolet
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Substrate Specificity
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Topoisomerase I Inhibitors
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Topoisomerase II Inhibitors
Substances
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Phenanthrolines
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Topoisomerase I Inhibitors
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Topoisomerase II Inhibitors
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DNA