Source:http://linkedlifedata.com/resource/pubmed/id/15109673
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
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pubmed:dateCreated |
2004-4-27
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pubmed:abstractText |
N-Ureido-quinoxalinedione derivatives have been discovered as leads for a novel series of dipeptidyl peptidase-IV (DPP-IV) inhibitors through high-throughput screening of our chemical library. A brief structure-activity relationship of the compounds was investigated. Among them, entry 5 showed the most potent inhibitory activity. The nitro group in quinoxaline moiety and the aromatic sulfonyl substituted ureido functional group seem to be important to increase the potency dramatically.
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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 |
May
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pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
17
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2661-4
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:15109673-Animals,
pubmed-meshheading:15109673-Automation,
pubmed-meshheading:15109673-Dipeptidyl Peptidase 4,
pubmed-meshheading:15109673-Protease Inhibitors,
pubmed-meshheading:15109673-Protein Array Analysis,
pubmed-meshheading:15109673-Quinoxalines,
pubmed-meshheading:15109673-Rats,
pubmed-meshheading:15109673-Structure-Activity Relationship
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pubmed:year |
2004
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pubmed:articleTitle |
Lead discovery of quinoxalinediones as an inhibitor of dipeptidyl peptidase-IV (DPP-IV) by high-throughput screening.
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pubmed:affiliation |
Biomedicinal Science Division, Korea Research Institute of Chemical Technology, PO Box 107, Yusung, Taejeon 305-706, South Korea.
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pubmed:publicationType |
Journal Article
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