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dc.contributor.authorKo, SB-
dc.contributor.authorLee, YS-
dc.contributor.authorLee, JY-
dc.contributor.authorHam, WH-
dc.contributor.authorPark, HK-
dc.date.accessioned2024-01-21T19:13:14Z-
dc.date.available2024-01-21T19:13:14Z-
dc.date.created2021-09-04-
dc.date.issued1996-10-
dc.identifier.issn0253-6269-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/144296-
dc.description.abstractA series of aminothiazolylcephalosporin derivatives (1a similar to 1c) having pyridinylethenyl group at C-3 position was prepared starting from phosphonium salt 3 and 2-, 3- or 4-pyridinecarboxaldehyde and the antibacterial activity of these compounds was investigated. Among them, 4-pyridinylethenyl derivative was more active than 2- and 3-pyridinylethenyl derivatives against Staphylococcus aureus and Escherichia coli.-
dc.languageEnglish-
dc.publisherPHARMACEUTICAL SOCIETY KOREA-
dc.titleSynthesis and biological activity of C-3 pyridinylethene-substituted cephalosporins-
dc.typeArticle-
dc.identifier.doi10.1007/BF02976388-
dc.description.journalClass1-
dc.identifier.bibliographicCitationARCHIVES OF PHARMACAL RESEARCH, v.19, no.5, pp.411 - 415-
dc.citation.titleARCHIVES OF PHARMACAL RESEARCH-
dc.citation.volume19-
dc.citation.number5-
dc.citation.startPage411-
dc.citation.endPage415-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1996VP91500014-
dc.identifier.scopusid2-s2.0-20544464466-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusESTERS-
dc.subject.keywordAuthorcephalosporins-
dc.subject.keywordAuthorantibacterial activity-
dc.subject.keywordAuthorpyridinylethenyl-
dc.subject.keywordAuthorWittig reaction-
dc.subject.keywordAuthorpyridinecarboxaldehyde-
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