Abstract
Iron chelators have emerged as a potential anti-cancer treatment strategy. In this study, a series of novel thiosemicarbazone iron chelators containing a quinoline scaffold were synthesized and characterized. A number of analogs show markedly greater anti-cancer activity than the 'gold-standard' iron chelator, desferrioxamine. The anti-proliferative activity and iron chelation efficacy of several of these ligands (especially compound 1b), indicates that further investigation of this class of thiosemicarbazones is worthwhile.
Copyright © 2012 Elsevier Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacology*
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Deferoxamine / pharmacology
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Humans
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Iron / metabolism
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Iron Chelating Agents / chemical synthesis
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Iron Chelating Agents / chemistry*
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Iron Chelating Agents / pharmacology*
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Neoplasms / drug therapy
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Neoplasms / metabolism
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Quinolines / chemical synthesis
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Quinolines / chemistry
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Quinolines / pharmacology
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Thiosemicarbazones / chemical synthesis
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Thiosemicarbazones / chemistry*
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Thiosemicarbazones / pharmacology*
Substances
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Antineoplastic Agents
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Iron Chelating Agents
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Quinolines
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Thiosemicarbazones
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Iron
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Deferoxamine