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rdf:type |
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|
lifeskim:mentions |
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pubmed:issue |
24
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pubmed:dateCreated |
1999-4-5
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pubmed:abstractText |
A series of trisubstituted hydantoins has been prepared by a versatile solid phase route employing primary alcohols, amines and amino acids as the monomeric building blocks. Several compounds showed submicromolar affinity in binding assays at recombinant human somatostatin receptors.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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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 |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
3609-14
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:9934480-Animals,
pubmed-meshheading:9934480-CHO Cells,
pubmed-meshheading:9934480-Cricetinae,
pubmed-meshheading:9934480-Humans,
pubmed-meshheading:9934480-Hydantoins,
pubmed-meshheading:9934480-Iodine Radioisotopes,
pubmed-meshheading:9934480-Ligands,
pubmed-meshheading:9934480-Radioligand Assay,
pubmed-meshheading:9934480-Receptors, Somatostatin,
pubmed-meshheading:9934480-Recombinant Proteins,
pubmed-meshheading:9934480-Somatostatin
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pubmed:year |
1998
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pubmed:articleTitle |
The solid phase synthesis of a series of tri-substituted hydantoin ligands for the somatostatin SST5 receptor.
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pubmed:affiliation |
Glaxo Wellcome Cambridge Chemistry Laboratory, University Chemical Laboratories, UK. jjs0985@glaxowellcome.co.uk
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pubmed:publicationType |
Journal Article
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