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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
24
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pubmed:dateCreated |
1999-4-5
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pubmed:abstractText |
A series of styrylpyridine derivatives containing two phenols was prepared via an efficient two-step synthesis. These compounds were designed to maximize the estrogen receptor binding affinity of a known series of inherently fluorescent styrylpyridines. While significant improvements were achieved in receptor affinity, the fluorescence intensity of this series of compounds is poor.
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pubmed:grant | |
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 |
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 |
3589-94
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:9934476-Fluorescent Dyes,
pubmed-meshheading:9934476-Ligands,
pubmed-meshheading:9934476-Magnetic Resonance Spectroscopy,
pubmed-meshheading:9934476-Protein Binding,
pubmed-meshheading:9934476-Pyridines,
pubmed-meshheading:9934476-Receptors, Estrogen,
pubmed-meshheading:9934476-Spectrometry, Fluorescence
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pubmed:year |
1998
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pubmed:articleTitle |
Facile synthesis of high affinity styrylpyridine systems as inherently fluorescent ligands for the estrogen receptor.
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pubmed:affiliation |
Department of Chemistry, University of Illinois, Urbana 61801, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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