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dc.contributor.authorKim, MJ-
dc.contributor.authorKim, HO-
dc.contributor.authorKim, HD-
dc.contributor.authorKim, JH-
dc.contributor.authorJeong, LS-
dc.contributor.authorChun, MW-
dc.date.accessioned2024-01-21T08:06:13Z-
dc.date.available2024-01-21T08:06:13Z-
dc.date.created2021-09-03-
dc.date.issued2003-10-20-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138140-
dc.description.abstractThe pyrimidine nucleosides fused with 3',4'-tetrahydrofuran ring were successfully synthesized, starting from 1,2;5,6-di-O-isopropylidene-D-glucose and assayed for antiviral activities against HIV-1, HIV-2, EMCV, Cox. B3 and VSV. Thymine analogue (5) and its corresponding 2'-deoxy analogue (6) exhibited high cytotoxicity instead of giving antiviral activities. (C) 2003 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.subjectANALOGS-
dc.titleSynthesis and biological evaluation of thymine nucleosides fused with 3 ',4 '-tetrahydrofuran ring-
dc.typeArticle-
dc.identifier.doi10.1016/S0960-894X(03)00730-3-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.13, no.20, pp.3499 - 3501-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume13-
dc.citation.number20-
dc.citation.startPage3499-
dc.citation.endPage3501-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000185590300023-
dc.identifier.scopusid2-s2.0-0141851413-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusANALOGS-
dc.subject.keywordAuthorthymine nucleosides-
dc.subject.keywordAuthortetrahydrofuran-
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