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dc.contributor.authorChun, MW-
dc.contributor.authorKim, MJ-
dc.contributor.authorKim, HO-
dc.contributor.authorMoon, HR-
dc.contributor.authorKim, HD-
dc.contributor.authorKim, JH-
dc.contributor.authorJeong, LS-
dc.date.accessioned2024-01-21T08:10:36Z-
dc.date.available2024-01-21T08:10:36Z-
dc.date.created2021-09-01-
dc.date.issued2003-10-
dc.identifier.issn1525-7770-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/138222-
dc.description.abstractPyrimidine nucleosides fused with 3,4'-tetrahydrofuran ring were synthesized, starting from 1,2;5,6-di-O-isopropylidene-D-glucose and assayed for antiviral activities. Thymine analogue 1 and its corresponding 2'-deoxy analogue 3 exhibited high cytotoxicity instead of giving antiviral activities.-
dc.languageEnglish-
dc.publisherMARCEL DEKKER INC-
dc.titleSynthesis and biological evaluation of pyrimidine nucleosides fused with 3 ',4 '-tetrahydrofuran ring-
dc.typeArticle-
dc.identifier.doi10.1081/NCN-120022618-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, v.22, no.5-8, pp.719 - 721-
dc.citation.titleNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS-
dc.citation.volume22-
dc.citation.number5-8-
dc.citation.startPage719-
dc.citation.endPage721-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000185439200038-
dc.identifier.scopusid2-s2.0-0141537183-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeArticle; Proceedings Paper-
dc.subject.keywordAuthorpyrimidine nucleosides-
dc.subject.keywordAuthortetrahydrofuran-
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KIST Article > 2003
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