Source:http://linkedlifedata.com/resource/pubmed/id/12873490
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
16
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pubmed:dateCreated |
2003-7-22
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pubmed:abstractText |
Suzuki cross-coupling has been used to access a wide range of 3- and 5-substituted 2-pyrones, which show remarkable inhibitory activity against bacteria, yeasts and fungi. 3-Octenyl and 5-octenyl 2-pyrones inhibit human ovarium carcinoma (A2780) and human chronic myelogenous leukaemia (K562) cell lines at the micromolar level.
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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 |
Aug
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
18
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2667-71
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12873490-Anti-Infective Agents,
pubmed-meshheading:12873490-Antineoplastic Agents,
pubmed-meshheading:12873490-Bacteria,
pubmed-meshheading:12873490-Boronic Acids,
pubmed-meshheading:12873490-Cell Line, Tumor,
pubmed-meshheading:12873490-Fungi,
pubmed-meshheading:12873490-Humans,
pubmed-meshheading:12873490-Models, Chemical,
pubmed-meshheading:12873490-Pyrones,
pubmed-meshheading:12873490-Structure-Activity Relationship
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pubmed:year |
2003
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pubmed:articleTitle |
Suzuki cross-coupling approaches to the synthesis of bioactive 3-substituted and 5-substituted-4-methoxy-6-methyl-2-pyrones.
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pubmed:affiliation |
Department of Chemistry and Materials, John Dalton Building, The Manchester Metropolitan University, Chester Street, Manchester M1 5GD, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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