Source:http://linkedlifedata.com/resource/pubmed/id/17448574
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11-12
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pubmed:dateCreated |
2007-11-26
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pubmed:abstractText |
The synthesis of 1-aryl-4,6-dihydropyrazolo[4,3-d][1]benzazepin-5(1H)-ones by cyclization of 4-[(dimethylamino)methylidene]-3,4-dihydro-1H-[1]benzazepine-2,5-dione with arylhydrazines is reported. When tested on a panel of human cancer cell lines, the title compounds showed antiproliferative activity and a characteristic selectivity pattern of growth inhibition. Although structurally akin to established kinase inhibitors, the new compounds did not exhibit noteworthy inhibitory activity when tested on an array of cancer-related kinases.
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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:issn |
0223-5234
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1317-24
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pubmed:meshHeading |
pubmed-meshheading:17448574-Benzazepines,
pubmed-meshheading:17448574-Breast Neoplasms,
pubmed-meshheading:17448574-Cell Line, Tumor,
pubmed-meshheading:17448574-Cell Proliferation,
pubmed-meshheading:17448574-Computational Biology,
pubmed-meshheading:17448574-Humans,
pubmed-meshheading:17448574-Indoles,
pubmed-meshheading:17448574-Inhibitory Concentration 50,
pubmed-meshheading:17448574-Leukemia,
pubmed-meshheading:17448574-Protein Kinase Inhibitors
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pubmed:articleTitle |
1-Aryl-4,6-dihydropyrazolo[4,3-d][1]benzazepin-5(1H)-ones: a new class of antiproliferative agents with selectivity for human leukemia and breast cancer cell lines.
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pubmed:affiliation |
Technische Universität Braunschweig, Institut für Pharmazeutische Chemie, Beethovenstrasse 55, D-38106 Braunschweig, Germany.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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