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DERIVATIVES OF 4-STYRYLPYRIDINES - SYNTHESIS, ESTROGEN-RECEPTOR BINDING-AFFINITY, AND PHOTOPHYSICAL PROPERTIES

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dc.contributor.author HAROUTOUNIAN, SA en
dc.contributor.author SCRIBNER, AW en
dc.contributor.author KATZENELLENBOGEN, JA en
dc.date.accessioned 2014-06-06T06:42:48Z
dc.date.available 2014-06-06T06:42:48Z
dc.date.issued 1995 en
dc.identifier.issn 0039-128X en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/818
dc.subject STYRYLPYRIDINES en
dc.subject FLUORESCENT ESTROGENS en
dc.subject ESTROGEN RECEPTOR BINDING en
dc.subject NONSTEROIDAL ESTROGENS en
dc.subject.classification Biochemistry & Molecular Biology en
dc.subject.classification Endocrinology & Metabolism en
dc.subject.other LIGAND en
dc.title DERIVATIVES OF 4-STYRYLPYRIDINES - SYNTHESIS, ESTROGEN-RECEPTOR BINDING-AFFINITY, AND PHOTOPHYSICAL PROPERTIES en
heal.type journalArticle en
heal.language English en
heal.publicationDate 1995 en
heal.abstract In order to develop novel ligands for the estrogen receptor (ER) that might have high binding affinity and fluorescence properties suitable for assaying ER levels in cells, we have prepared a series of substituted 4'-hydroxyl-styrylpyridines and phenylethylpyridines and studied their optical spectroscopy and receptor binding properties. Several derivatives that contain alkyl substituents on the internal ethene or ethane carbons were prepared. While most of these compounds have only modest affinity for ER, one fluorescent analog, (E)-1-(4-hydroxyphenyl)-1-phenyl-2-(4-pyridinyl)ethene (13), has reasonably good binding affinity for ER and shows long wavelength fluorescence emission that is sensitive to solvent polarity and pH. This compound may prove to be a useful probe for detecting ER in cells. en
heal.publisher BUTTERWORTH-HEINEMANN en
heal.journalName STEROIDS en
dc.identifier.issue 9 en
dc.identifier.volume 60 en
dc.identifier.isi ISI:A1995RR54200006 en
dc.identifier.spage 636 en
dc.identifier.epage 645 en


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