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dc.contributor.author이강만-
dc.contributor.author정낙신-
dc.contributor.author이상국-
dc.date.accessioned2018-05-30T08:14:29Z-
dc.date.available2018-05-30T08:14:29Z-
dc.date.issued2005-
dc.identifier.issn1525-7770-
dc.identifier.otherOAK-2942-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243663-
dc.description.abstractFour 5′-substituted fluoro-neplanocin A analogues 1a-d were designed and synthesized, and the inhibitory activity against SAH was in the following order: NH2 > SH > F, N3, indicating a hydrogen bonding donor is essential for inhibitory activity. Copyright © Taylor & Francis, Inc.-
dc.languageEnglish-
dc.titleStructure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase-
dc.typeConference Paper-
dc.relation.issue41401-
dc.relation.volume24-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage707-
dc.relation.lastpage708-
dc.relation.journaltitleNucleosides, Nucleotides and Nucleic Acids-
dc.identifier.doi10.1081/NCN-200060286-
dc.identifier.wosidWOS:000232473500074-
dc.identifier.scopusid2-s2.0-26644432957-
dc.author.googleMoon H.R.-
dc.author.googleLee K.M.-
dc.author.googleLee H.J.-
dc.author.googleLee S.K.-
dc.author.googlePark S.B.-
dc.author.googleChun M.W.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid이강만(7501506362)-
dc.contributor.scopusid정낙신(16028528200)-
dc.contributor.scopusid이상국(36067620500)-
dc.date.modifydate20211210153309-
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약학대학 > 약학과 > Journal papers
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