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dc.contributor.authorJung, KE-
dc.contributor.authorKang, YK-
dc.contributor.authorKim, DJ-
dc.contributor.authorPark, SW-
dc.date.accessioned2024-01-21T18:10:17Z-
dc.date.available2024-01-21T18:10:17Z-
dc.date.created2021-09-04-
dc.date.issued1997-08-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143689-
dc.description.abstractThe synthesis of cis- and trans-1,6-dihydroxypyrrolizidine starting from trans-4-hydroxy-L-proline and their evaluation as glycosidase inhibitors are reported. The cis-isomer was found to be a potent inhibitor against alpha-glucosidase and showed weak inhibitory effect against other glycosidases. The trans-isomer exhibited weak inhibitions of b-glucosidase and amyloglucosidase and poor inhibition of other glycosidases.-
dc.languageEnglish-
dc.publisherPHARMACEUTICAL SOCIETY KOREA-
dc.titleSynthesis and activity of a potent alpha-glucosidase inhibitor, (1R, 6R, 8S)-cis-1,6-dihydroxypyrrolizidine, and its isomer-
dc.typeArticle-
dc.identifier.doi10.1007/BF02976198-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIVES OF PHARMACAL RESEARCH, v.20, no.4, pp.346 - 350-
dc.citation.titleARCHIVES OF PHARMACAL RESEARCH-
dc.citation.volume20-
dc.citation.number4-
dc.citation.startPage346-
dc.citation.endPage350-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997XT70700009-
dc.identifier.scopusid2-s2.0-20544461663-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusAMYLOGLUCOSIDASE-
dc.subject.keywordPlusMANNOSIDASE-
dc.subject.keywordPlusSWAINSONINE-
dc.subject.keywordPlusAUSTRALINE-
dc.subject.keywordAuthorpyrrolizidine derivatives-
dc.subject.keywordAuthoralpha-glucosidase inhibitor-
dc.subject.keywordAuthorswainsonine-
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