Source:http://linkedlifedata.com/resource/pubmed/id/17507221
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
14
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pubmed:dateCreated |
2007-6-22
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pubmed:abstractText |
A novel class of non-peptide somatostatin receptor ligands bearing the octahydrobenzo[g]quinoline (obeline) structural element has been identified. SAR studies have been performed that led to the discovery of derivatives with high affinity (pK(d) r sst(1) > or = 9) and selectivity (> or = 150-fold for h sst(1) over h sst(2)-h sst(5)) for somatostatin receptor subtype sst(1). In a functional assay, the compounds act as antagonists at human recombinant sst(1) receptors.
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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 |
Jul
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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 |
17
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3983-7
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pubmed:meshHeading |
pubmed-meshheading:17507221-Animals,
pubmed-meshheading:17507221-Humans,
pubmed-meshheading:17507221-Luminescent Proteins,
pubmed-meshheading:17507221-Rats,
pubmed-meshheading:17507221-Receptors, Somatostatin,
pubmed-meshheading:17507221-Recombinant Proteins,
pubmed-meshheading:17507221-Structure-Activity Relationship
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pubmed:year |
2007
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pubmed:articleTitle |
Identification and SAR of potent and selective non-peptide obeline somatostatin sst1 receptor antagonists.
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pubmed:affiliation |
Novartis Institutes for BioMedical Research, CH-4002 Basel, Switzerland. thomas.troxler@novartis.com
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pubmed:publicationType |
Journal Article
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