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dc.contributor.author정낙신-
dc.date.accessioned2016-08-28T12:08:09Z-
dc.date.available2016-08-28T12:08:09Z-
dc.date.issued2008-
dc.identifier.issn0253-2964-
dc.identifier.otherOAK-5319-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220120-
dc.description.abstract5''-Iodoneplanocin A (1) and its analogues 2 and 3 were designed and synthesized as potential SAHH inhibitor via iodocyclopentenol 6, which was prepared using a Michael addition-iodination-elimination process. All final compounds did not show antiviral activity, maybe due to a steric hindrance induced by 5″-iodo substituent.-
dc.languageEnglish-
dc.titleDesign and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor-
dc.typeArticle-
dc.relation.issue12-
dc.relation.volume29-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.indexKCI-
dc.relation.startpage2487-
dc.relation.lastpage2490-
dc.relation.journaltitleBulletin of the Korean Chemical Society-
dc.identifier.wosidWOS:000262397500036-
dc.identifier.scopusid2-s2.0-60149106127-
dc.author.googlePark A.-Y.-
dc.author.googleKim K.R.-
dc.author.googleLee H.-R.-
dc.author.googleKang J.-A.-
dc.author.googleKim W.H.-
dc.author.googleChun P.-
dc.author.googleAhmad P.-
dc.author.googleJeong L.S.-
dc.author.googleMoon H.R.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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