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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2008-1-18
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pubmed:abstractText |
The design of novel Fe chelators with high Fe mobilization efficacy and low toxicity remains an important priority for the treatment of Fe overload disease. We have designed and synthesized the novel methyl pyrazinylketone isonicotinoyl hydrazone (HMPIH) analogs based on previously investigated aroylhydrazone chelators. The HMPIH series demonstrated high Fe mobilization efficacy from cells and showed limited to moderate antiproliferative activity. Importantly, this novel series demonstrated irreversible electrochemistry, which was attributed to the electron-withdrawing effects of the noncoordinating pyrazine N-atom. The latter functionality played a major role in forming redox-inactive complexes that prevent reactive oxygen species generation. In fact, the Fe complexes of the HMPIH series prevented the oxidation of ascorbate and hydroxylation of benzoate. We determined that the incorporation of electron-withdrawing groups is an important feature in the design of N, N, O-aroylhydrazones as candidate drugs for the treatment of Fe overload disease.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Ascorbic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Benzoates,
http://linkedlifedata.com/resource/pubmed/chemical/Hydrazones,
http://linkedlifedata.com/resource/pubmed/chemical/Iron,
http://linkedlifedata.com/resource/pubmed/chemical/Iron Chelating Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Iron Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Isonicotinic Acids,
http://linkedlifedata.com/resource/pubmed/chemical/Ketones,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrazines
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0022-2623
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
51
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
331-44
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pubmed:meshHeading |
pubmed-meshheading:18159922-Antineoplastic Agents,
pubmed-meshheading:18159922-Ascorbic Acid,
pubmed-meshheading:18159922-Benzoates,
pubmed-meshheading:18159922-Cell Line, Tumor,
pubmed-meshheading:18159922-Cell Proliferation,
pubmed-meshheading:18159922-Crystallography, X-Ray,
pubmed-meshheading:18159922-Humans,
pubmed-meshheading:18159922-Hydrazones,
pubmed-meshheading:18159922-Hydroxylation,
pubmed-meshheading:18159922-Iron,
pubmed-meshheading:18159922-Iron Chelating Agents,
pubmed-meshheading:18159922-Iron Overload,
pubmed-meshheading:18159922-Iron Radioisotopes,
pubmed-meshheading:18159922-Isonicotinic Acids,
pubmed-meshheading:18159922-Ketones,
pubmed-meshheading:18159922-Ligands,
pubmed-meshheading:18159922-Oxidation-Reduction,
pubmed-meshheading:18159922-Pyrazines,
pubmed-meshheading:18159922-Structure-Activity Relationship
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pubmed:year |
2008
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pubmed:articleTitle |
Structure-activity relationships of novel iron chelators for the treatment of iron overload disease: the methyl pyrazinylketone isonicotinoyl hydrazone series.
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pubmed:affiliation |
Iron Metabolism and Chelation Program, Department of Pathology, University of Sydney, Sydney, New South Wales 2006, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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