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Ultrasound-promoted synthesis of 2,3-bis(4-hydroxyphenyl)indole derivatives as inherently fluorescent ligands for the estrogen receptor

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dc.contributor.author Koulocheri, SD en
dc.contributor.author Haroutounian, SA en
dc.date.accessioned 2014-06-06T06:44:27Z
dc.date.available 2014-06-06T06:44:27Z
dc.date.issued 2001 en
dc.identifier.issn 1434193X en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/1888
dc.relation.uri http://www.scopus.com/inward/record.url?eid=2-s2.0-0035034612&partnerID=40&md5=41d53c3f222eb69a573827f213c35e29 en
dc.subject Cyclization en
dc.subject Estrogen receptor en
dc.subject Indoles en
dc.subject Ultrasound en
dc.subject.other 2,3 bis(4 hydroxyphenyl)indole en
dc.subject.other estrogen receptor en
dc.subject.other indole derivative en
dc.subject.other unclassified drug en
dc.subject.other article en
dc.subject.other binding site en
dc.subject.other derivatization en
dc.subject.other drug isolation en
dc.subject.other flow cytometry en
dc.subject.other ligand binding en
dc.subject.other receptor binding en
dc.subject.other structure analysis en
dc.subject.other synthesis en
dc.subject.other ultrasound en
dc.title Ultrasound-promoted synthesis of 2,3-bis(4-hydroxyphenyl)indole derivatives as inherently fluorescent ligands for the estrogen receptor en
heal.type journalArticle en
heal.publicationDate 2001 en
heal.abstract A series of 2,3-bis(4-hydroxyphenyl)indole derivatives 4c-f was prepared by ultrasound-promoted intramolecular cyclodehydration of a polyphosphoric acid solution of α-anilinyl-(or 3-anisidyl)desoxyanisoins 2c-f, and their optical spectroscopy and estrogen receptor (ER) binding properties were studied. Compounds 4c-f give intense long-wavelength fluorescent emission, sensitive to solvent polarity and pH. Furthermore, the two indol-6-ols 4e, f display reasonably good binding affinities to ER and appear to be well suited for use as fluorescent probes for the detection of ER in cells. en
heal.journalName European Journal of Organic Chemistry en
dc.identifier.issue 9 en
dc.identifier.spage 1723 en
dc.identifier.epage 1729 en


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