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dc.contributor.authorKim, SN-
dc.contributor.authorLee, JY-
dc.contributor.authorKim, HJ-
dc.contributor.authorShin, CG-
dc.contributor.authorPark, H-
dc.contributor.authorLee, YS-
dc.date.accessioned2024-01-21T13:38:02Z-
dc.date.available2024-01-21T13:38:02Z-
dc.date.created2021-09-05-
dc.date.issued2000-08-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/141163-
dc.description.abstractCaffeoylglucosides, which have a glucose ring as a central linker, were synthesized from methyl D-glucosides, and their anti-HIV-1 activities were tested. Among them, four dicaffeoylglucosides (IC50 = 29.1-35.1 mu M), 6a, 6b, 9b and 10b, showed HIV-1 integrase inhibitory activity as potent as L-chicoric acid. (C) 2000 Elsevier Science Ltd. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleSynthesis and HIV-1 integrase inhibitory activities of caffeoylglucosides-
dc.typeArticle-
dc.identifier.doi10.1016/S0960-894X(00)00355-3-
dc.description.journalClass1-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.10, no.16, pp.1879 - 1882-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume10-
dc.citation.number16-
dc.citation.startPage1879-
dc.citation.endPage1882-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000088837600025-
dc.identifier.scopusid2-s2.0-0034698891-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.type.docTypeArticle-
dc.subject.keywordPlusIMMUNODEFICIENCY-VIRUS TYPE-1-
dc.subject.keywordPlusDICAFFEOYLTARTARIC ACIDS-
dc.subject.keywordPlusPOTENT INHIBITORS-
dc.subject.keywordPlusREPLICATION-
dc.subject.keywordPlusANALOGS-
dc.subject.keywordAuthorAIDS-
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