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dc.contributor.author권영주*
dc.date.accessioned2017-02-15T08:02:04Z-
dc.date.available2017-02-15T08:02:04Z-
dc.date.issued2007*
dc.identifier.issn0960-894X*
dc.identifier.otherOAK-3877*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/234272-
dc.description.abstractIn this report, we prepared some 3-(2′,3′-epoxypropoxy)xanthones and their epoxide ring opened halohydrin analogues, and evaluated their cytotoxicity and topoisomerase II inhibition activity using doxorubicin and etoposide as references, respectively. Another xanthone compound 9, 1,3-di(2′,3′-epoxypropoxy)xanthone, was also synthesized and its DNA cross-linking property including other two biological activities investigated. The biological test results showed compound 9 possessed excellent cytotoxic and topoisomerase II inhibitory activity than other compounds tested. It also exhibited significant DNA cross-linking activities. © 2006 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSynthesis of new xanthone analogues and their biological activity test-Cytotoxicity, topoisomerase II inhibition, and DNA cross-linking study*
dc.typeArticle*
dc.relation.issue5*
dc.relation.volume17*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1163*
dc.relation.lastpage1166*
dc.relation.journaltitleBioorganic and Medicinal Chemistry Letters*
dc.identifier.doi10.1016/j.bmcl.2006.12.030*
dc.identifier.wosidWOS:000244943300004*
dc.identifier.scopusid2-s2.0-33846898056*
dc.author.googleWoo S.*
dc.author.googleJung J.*
dc.author.googleLee C.*
dc.author.googleKwon Y.*
dc.author.googleNa Y.*
dc.contributor.scopusid권영주(12446435600)*
dc.date.modifydate20240422124907*
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약학대학 > 약학과 > Journal papers
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