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Cited 68 time in webofscience Cited 73 time in scopus
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dc.contributor.authorYi, JW-
dc.contributor.authorBarry, NPE-
dc.contributor.authorFurrer, MA-
dc.contributor.authorZava, O-
dc.contributor.authorDyson, PJ-
dc.contributor.authorTherrien, B-
dc.contributor.authorKim, BH-
dc.date.accessioned2016-03-31T08:57:37Z-
dc.date.available2016-03-31T08:57:37Z-
dc.date.created2012-08-10-
dc.date.issued2012-03-
dc.identifier.issn1043-1802-
dc.identifier.other2012-OAK-0000025735-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/16377-
dc.description.abstractThe self-assembly of 2,4,6-tris(pyridin-4-yl)-1,3,5-triazine (tpt) triangular panels with p-cymene (pPr(i)C(6)H(4)Me) ruthenium building blocks and 2,5-dioxydo-1,4-benzoquinonato (dobq) or 5,8-dioxydo-1,4-naphthoquinonato (donq) bridges, in the presence of a pyrenyl-nucleoside derivatives (pyreneR),. affords the triangular prismatic host guest compounds [(pyrene-R)CRu6(pPr(i)C(6)H(4)Me)(6)(tpt)(2)(dobq)(3)](6+) ([(pyrene-R)C1](6+)) and [(pyrene-R)CRu6(pPr(i)C(6)H(4)Me)(6)(tpt)(2)(donq)(3)](6+) ([(pyrene-R)C2](6+)), respectively. The inclusion of six monosubstituted pyrenyl-nucleosides (pyrene-R1 = 5'-(1-pyrenyl butanoate)-2'-deoxyuridine, pyrene-R2 = 5-fluoro-5'-(1-pyrenyl butanoate)-2'-deoxyuridine, pyrene-R3 = 5'-{N-[1-oxo-4-(1-pyrenyl)butyl]glycyl}-2'-deoxyuridine, pyrene-R4 = 5-fluoro-5'-{N[1-oxo-4-(1-pyrenyl)butyl]-glycyl}2'-deoxyuridine, pyrene-R5 = 5-fluoro-5'-{N-[1-oxo-4-(1-pyrenyl)butyl]-phenylalanyl}-2'-deoxyvuridine, pyrene-R6 = 5-fluoro-5'-{N-[1-oxo-4-(1-pyrenyl)butyl]-phenylalanyl}-2'-deoxyuridine) has been accomplished. The carceplex nature of [(pyrene-R)C1](6+) with the pyrenyl moiety firmly encapsulated in the hydrophobic cavity of the cage with the nucleoside groups pointing outward was confirmed by NMR spectroscopy and electrospray ionization mass spectrometry (ESI-MS), while the host-guest nature of [(pyrene-R)C2](6+) was studied in solution by NMR techniques. In contrast to the floxuridine compounds used in the clinic, the host-guest complexes are highly water-soluble. Consequently, the cytotoxicities of these water-soluble compounds have been established using human ovarian A2780 and A2780cisR cancer cells. All the host guest systems are more cytotoxic than the empty cages alone [1][CF3SO3](6) (IC50 = 23 mu M) and [2][CF3SO3](6) (IC50 = 10 mu M), the most active compound [pyrene-R4C1][CF3SO3](6) being 2 orders of magnitude more cytotoxic (IC50 = 0.3 mu M) on these human ovarian cancer cell lines (A2780 and A2780cisR).-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherAmerican Chemical Society-
dc.relation.isPartOfBIOCONJUGATE CHEMISTRY-
dc.subjectRUTHENIUM COMPLEXES-
dc.subjectANTICANCER ACTIVITY-
dc.subjectNUCLEOSIDE ANALOGS-
dc.subjectDRUG-RELEASE-
dc.subjectPRODRUGS-
dc.subject5-FLUOROURACIL-
dc.subjectENCAPSULATION-
dc.subjectPERMEABILITY-
dc.subjectMECHANISMS-
dc.subjectSTRATEGIES-
dc.titleDelivery of Floxuridine Derivatives to Cancer Cells by Water-Soluble Organometallic Cages-
dc.typeArticle-
dc.contributor.college융합생명공학부-
dc.identifier.doi10.1021/bc200472n-
dc.author.googleYi, JW-
dc.author.googleBarry, NPE-
dc.author.googleFurrer, MA-
dc.author.googleZava, O-
dc.author.googleDyson, PJ-
dc.author.googleTherrien, B-
dc.relation.volume23-
dc.relation.issue3-
dc.relation.startpage461-
dc.relation.lastpage471-
dc.contributor.id10142056-
dc.relation.journalBIOCONJUGATE CHEMISTRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCONJUGATE CHEMISTRY, v.23, no.3, pp.461 - 471-
dc.identifier.wosid000301700200017-
dc.date.tcdate2019-01-01-
dc.citation.endPage471-
dc.citation.number3-
dc.citation.startPage461-
dc.citation.titleBIOCONJUGATE CHEMISTRY-
dc.citation.volume23-
dc.contributor.affiliatedAuthorKim, BH-
dc.identifier.scopusid2-s2.0-84863337900-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc44-
dc.type.docTypeArticle-
dc.subject.keywordPlusRUTHENIUM COMPLEXES-
dc.subject.keywordPlusDRUG-RELEASE-
dc.subject.keywordPlusANTICANCER-
dc.subject.keywordPlusPRODRUGS-
dc.subject.keywordPlus5-FLUOROURACIL-
dc.subject.keywordPlusENCAPSULATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusRESISTANCE-
dc.relation.journalWebOfScienceCategoryBiochemical Research Methods-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-

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김병현KIM, BYEANG HYEAN
Div of Advanced Materials Science
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