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Cited 76 time in webofscience Cited 79 time in scopus
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dc.contributor.authorLi, Qian-
dc.contributor.authorMin, Jaeki-
dc.contributor.authorAhn, Young-Hoon-
dc.contributor.authorNamm, Joshua-
dc.contributor.authorKim, Eun Min-
dc.contributor.authorLui, Rowena-
dc.contributor.authorKim, Hye Yun-
dc.contributor.authorJi, Yong-
dc.contributor.authorWu, Hueizhi-
dc.contributor.authorWisniewski, Thomas-
dc.contributor.authorChang, Young-Tae-
dc.date.accessioned2018-06-15T05:14:38Z-
dc.date.available2018-06-15T05:14:38Z-
dc.date.created2017-09-08-
dc.date.issued2007-09-
dc.identifier.issn1439-4227-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/50253-
dc.description.abstractA group of styryl-based neutral compounds has been synthesized in this study for potential use as in vivo imaging agents for beta-amyloid plaques. Of 56 candidates, 14 compounds were found to label beta-amyloid plaques well on Alzheimer's disease (AD) human brain sections in vitro. The binding affinity to beta-amyloid fibrils was then determined by measuring the change in fluorescence intensity. Interestingly, we found that a class of quinaldine-styryl scaffold compounds displays specific binding to beta-amyloid fibrils. A representative compound, STB-8, was used in ex vivo and in vivo imaging experiments on an AD transgenic mouse model and demonstrated excellent blood-brain barrier (BBB) permeability and specific staining of the AD beta-amyloid plaques.-
dc.languageEnglish-
dc.publisherWILEY-V C H VERLAG GMBH-
dc.relation.isPartOfCHEMBIOCHEM-
dc.subjectPOSITRON-EMISSION-TOMOGRAPHY-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectCONGO-RED-
dc.subjectBENZOFURAN DERIVATIVES-
dc.subjectPEPTIDE FIBRILS-
dc.subjectBINDING-SITES-
dc.subjectCHRYSAMINE-G-
dc.subjectBRAIN-
dc.subjectDEPOSITS-
dc.subjectPROBES-
dc.titleStyryl-based compounds as potential in vivo imaging agents for beta-amyloid plaques-
dc.typeArticle-
dc.identifier.doi10.1002/cbic.200700154-
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMBIOCHEM, v.8, no.14, pp.1679 - 1687-
dc.identifier.wosid000249912100012-
dc.date.tcdate2019-02-01-
dc.citation.endPage1687-
dc.citation.number14-
dc.citation.startPage1679-
dc.citation.titleCHEMBIOCHEM-
dc.citation.volume8-
dc.contributor.affiliatedAuthorChang, Young-Tae-
dc.identifier.scopusid2-s2.0-34948887647-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc50-
dc.type.docTypeArticle-
dc.subject.keywordPlusPOSITRON-EMISSION-TOMOGRAPHY-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusCONGO-RED-
dc.subject.keywordPlusBENZOFURAN DERIVATIVES-
dc.subject.keywordPlusPEPTIDE FIBRILS-
dc.subject.keywordPlusBINDING-SITES-
dc.subject.keywordPlusCHRYSAMINE-G-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusDEPOSITS-
dc.subject.keywordPlusPROBES-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaPharmacology & Pharmacy-

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