Source:http://linkedlifedata.com/resource/pubmed/id/16890431
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
20
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pubmed:dateCreated |
2006-9-11
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pubmed:abstractText |
Synthetic routes towards highly substituted eight membered ring heterocycles fused to aryl rings such as the dibenzo[b,f]azocine system are still lacking. Herein, we present a convenient convergent synthetic route towards this heterocyclic class of compounds with possible variations at positions 4, 7, and 11. One member of a library of dibenzo[b,f]azocines with different substituents at position 11 was identified to inhibit protein kinase A activity (IC(50)=122microM) but not protein kinase C.
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pubmed:grant | |
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 |
Oct
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5360-3
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:16890431-Azocines,
pubmed-meshheading:16890431-Drug Evaluation, Preclinical,
pubmed-meshheading:16890431-Enzyme Activation,
pubmed-meshheading:16890431-Molecular Structure,
pubmed-meshheading:16890431-Protein Kinase Inhibitors,
pubmed-meshheading:16890431-Protein Kinases,
pubmed-meshheading:16890431-Stereoisomerism,
pubmed-meshheading:16890431-Structure-Activity Relationship,
pubmed-meshheading:16890431-Substrate Specificity
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pubmed:year |
2006
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pubmed:articleTitle |
Synthesis of highly substituted dibenzo[b,f]azocines and their evaluation as protein kinase inhibitors.
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pubmed:affiliation |
St. Jude Children's Research Hospital, Department of Chemical Biology and Therapeutics, 332 N. Lauderdale St., Memphis, TN 38105-2794, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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