Source:http://linkedlifedata.com/resource/pubmed/id/16143523
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
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pubmed:dateCreated |
2005-9-26
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pubmed:abstractText |
A novel series of inhibitors of cancer cell proliferation, selective against p21 cell cycle checkpoint-disrupted cells vs. cells with intact p21 checkpoint, were identified by high-throughput screening. Optimization of both ends of the lead molecule to improve potency, using parallel synthesis and iterative design, is described. The 2-(1,4-dibenzodioxane)-substituted derivative 14 was identified as a highly selective and potent agent displaying an IC50 of 91 nM in the p21-deficient cell line.
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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 |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4731-5
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pubmed:meshHeading |
pubmed-meshheading:16143523-Antineoplastic Agents,
pubmed-meshheading:16143523-Cell Line, Tumor,
pubmed-meshheading:16143523-Cell Proliferation,
pubmed-meshheading:16143523-Humans,
pubmed-meshheading:16143523-Inhibitory Concentration 50,
pubmed-meshheading:16143523-Pyrimidinones,
pubmed-meshheading:16143523-Structure-Activity Relationship,
pubmed-meshheading:16143523-Tubulin
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pubmed:year |
2005
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pubmed:articleTitle |
Parallel synthesis and biological evaluation of 5,6,7,8-tetrahydrobenzothieno[2,3-d]pyrimidin-4(3H)-one cytotoxic agents selective for p21-deficient cells.
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pubmed:affiliation |
Department of Exploratory Chemistry, Wyeth Research, Pearl River, NY 10965, USA. jenninl@wyeth.com
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pubmed:publicationType |
Journal Article
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