Source:http://linkedlifedata.com/resource/pubmed/id/18839938
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2008-11-6
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pubmed:abstractText |
Novel structural analogues of a HDAC inhibitor FK228 have been synthesized by modifying the most synthetically challenging unit, (3 S,4 E)-3-hydroxy-7-mercaptoheptenoic acid, with simple isosteric substitutions. These changes did not alter the backbone structure from FK228 but enabled facile and rapid synthesis by using readily available starting materials and high-yielding reactions. FK228 analogues were examined for their antitumoral activity on a variety of human cancer cells and led to the identification of new potent compounds.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1520-4804
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
13
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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 |
6639-41
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pubmed:meshHeading |
pubmed-meshheading:18839938-Antineoplastic Agents,
pubmed-meshheading:18839938-Cell Line, Tumor,
pubmed-meshheading:18839938-Cell Proliferation,
pubmed-meshheading:18839938-Depsipeptides,
pubmed-meshheading:18839938-Humans,
pubmed-meshheading:18839938-Models, Molecular,
pubmed-meshheading:18839938-Molecular Structure,
pubmed-meshheading:18839938-Structure-Activity Relationship
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pubmed:year |
2008
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pubmed:articleTitle |
Efficient solid-phase synthesis of FK228 analogues as potent antitumoral agents.
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pubmed:affiliation |
Department of Chemistry, University of Texas at Dallas, Richardson, Texas 75080, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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