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dc.contributor.authorChang, MH-
dc.contributor.authorKoh, HY-
dc.contributor.authorCho, YS-
dc.contributor.authorChoi, KI-
dc.date.accessioned2024-01-21T18:34:56Z-
dc.date.available2024-01-21T18:34:56Z-
dc.date.created2021-09-05-
dc.date.issued1997-04-
dc.identifier.issn1381-6128-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/143875-
dc.description.abstractSince the catechol type cephalosporins having a potent activity against P. aeruginosa strain were introduced, many kinds of derivatives have been developed. These cephalosporins adopted various substituents as siderophores such as catechol or pyridone type derivatives at C-7 or C-3 position to facilitate their penetration through the bacterial cell membrane. In this review, the structural specifications of the recently developed cephalosporins and their biological activity against P. aeruginosa bacterial strain would be overviewed.-
dc.languageEnglish-
dc.publisherBENTHAM SCIENCE PUBL BV-
dc.subjectANTIBACTERIAL ACTIVITY-
dc.subjectSYNTHETIC CEPHALOSPORINS-
dc.subjectCATECHOL MOIETY-
dc.subjectC-7-
dc.subjectPOSITION-
dc.subjectACID-
dc.titleNovel anti-pseudomonas cephalosporins-
dc.typeArticle-
dc.description.journalClass1-
dc.identifier.bibliographicCitationCURRENT PHARMACEUTICAL DESIGN, v.3, no.2, pp.209 - 226-
dc.citation.titleCURRENT PHARMACEUTICAL DESIGN-
dc.citation.volume3-
dc.citation.number2-
dc.citation.startPage209-
dc.citation.endPage226-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosidA1997XD39300007-
dc.identifier.scopusid2-s2.0-0030953133-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeReview-
dc.subject.keywordPlusANTIBACTERIAL ACTIVITY-
dc.subject.keywordPlusSYNTHETIC CEPHALOSPORINS-
dc.subject.keywordPlusCATECHOL MOIETY-
dc.subject.keywordPlusC-7-
dc.subject.keywordPlusPOSITION-
dc.subject.keywordPlusACID-
dc.subject.keywordAuthorreview-
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