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dc.contributor.author이상국-
dc.date.accessioned2016-08-28T12:08:36Z-
dc.date.available2016-08-28T12:08:36Z-
dc.date.issued2007-
dc.identifier.issn0960-894X-
dc.identifier.otherOAK-3785-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/219806-
dc.description.abstractDue to the profound cytotoxicities and interesting biochemical aspects, phenanthroindolizidine alkaloids have received an attention as potential therapeutic leads. To define the features of the molecule that are essential for cytotoxicity, we have synthesized and evaluated a series of phenanthroindolizidine alkaloid, antofine, analogues with different substituents on the phenanthrene ring. The systematic structure activity relationship studies elucidate the essential functional group requirement of phenanthrene ring, providing the basis for further development of phenanthroindolizidine alkaloids. © 2006 Elsevier Ltd. All rights reserved.-
dc.languageEnglish-
dc.titleSynthesis and structure-activity studies of antofine analogues as potential anticancer agents-
dc.typeArticle-
dc.relation.issue1-
dc.relation.volume17-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage97-
dc.relation.lastpage100-
dc.relation.journaltitleBioorganic and Medicinal Chemistry Letters-
dc.identifier.doi10.1016/j.bmcl.2006.09.080-
dc.identifier.wosidWOS:000243630500017-
dc.identifier.scopusid2-s2.0-33845762339-
dc.author.googleFu Y.-
dc.author.googleLee S.K.-
dc.author.googleMin H.-Y.-
dc.author.googleLee T.-
dc.author.googleLee J.-
dc.author.googleCheng M.-
dc.author.googleKim S.-
dc.contributor.scopusid이상국(36067620500)-
dc.date.modifydate20211210153309-
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약학대학 > 약학과 > Journal papers
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