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dc.contributor.authorLee, JY-
dc.contributor.authorOh, CH-
dc.contributor.authorKo, OH-
dc.contributor.authorHong, JH-
dc.date.accessioned2024-01-21T09:39:11Z-
dc.date.available2024-01-21T09:39:11Z-
dc.date.created2022-01-10-
dc.date.issued2002-12-
dc.identifier.issn1525-7770-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/139005-
dc.description.abstractA series of novel acyclic nucleosides 10, 11, 21, and 22 were synthesized efficiently starting from D-lactose. The condensation of the mesylate 5 and 16 with an adenine and cytosine base under standard nucleophilic substitution conditions (K2CO3, 18-Crown-6, DMF) afforded a series of acyclic novel nucleosides. Compound 21 displayed moderate anti-HCMV activity in the AD-169 cells (EC50 = 18.5 mug/mL) without exhibiting any cytotoxicity up to 100 muM.-
dc.languageEnglish-
dc.publisherTAYLOR & FRANCIS INC-
dc.subjectSIMPLEX VIRUS TYPE-1-
dc.subjectANTIVIRAL ACTIVITY-
dc.subjectANALOGS-
dc.titleSynthesis and anti-HCMV activity of novel acyclic nucleosides-
dc.typeArticle-
dc.identifier.doi10.1081/NCN-120015727-
dc.description.journalClass1-
dc.identifier.bibliographicCitationNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, v.21, no.10, pp.709 - 721-
dc.citation.titleNUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS-
dc.citation.volume21-
dc.citation.number10-
dc.citation.startPage709-
dc.citation.endPage721-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000179627900007-
dc.identifier.scopusid2-s2.0-1842869980-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.type.docTypeArticle-
dc.subject.keywordPlusSIMPLEX VIRUS TYPE-1-
dc.subject.keywordPlusANTIVIRAL ACTIVITY-
dc.subject.keywordPlusANALOGS-
dc.subject.keywordAuthornucleoside-
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