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dc.contributor.author정낙신-
dc.contributor.author최원준-
dc.date.accessioned2016-08-28T12:08:21Z-
dc.date.available2016-08-28T12:08:21Z-
dc.date.issued2012-
dc.identifier.issn0022-2623-
dc.identifier.otherOAK-8767-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/222631-
dc.description.abstractOn the basis of the potent biological activity of cyclopentenyl- pyrimidines, fluorocyclopentenyl-pyrimidines were designed and synthesized from d-ribose. Among these, the cytosine derivative 5a showed highly potent antigrowth effects in a broad range of tumor cell lines and very potent antitumor activity in a nude mouse tumor xenograft model implanted with A549 human lung cancer cells. However, its 2′-deoxycytidine derivative 5b did not show any antigrowth effects, indicating that 2′-hydroxyl group is essential for the biological activity. © 2012 American Chemical Society.-
dc.languageEnglish-
dc.titleFluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity-
dc.typeArticle-
dc.relation.issue9-
dc.relation.volume55-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage4521-
dc.relation.lastpage4525-
dc.relation.journaltitleJournal of Medicinal Chemistry-
dc.identifier.doi10.1021/jm3004009-
dc.identifier.wosidWOS:000303785900039-
dc.identifier.scopusid2-s2.0-84861028393-
dc.author.googleChoi W.J.-
dc.author.googleChung H.-J.-
dc.author.googleChandra G.-
dc.author.googleAlexander V.-
dc.author.googleZhao L.X.-
dc.author.googleLee H.W.-
dc.author.googleNayak A.-
dc.author.googleMajik M.S.-
dc.author.googleKim H.O.-
dc.author.googleKim J.-H.-
dc.author.googleLee Y.B.-
dc.author.googleAhn C.H.-
dc.author.googleLee S.K.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.contributor.scopusid최원준(55732412300;57211762651)-
dc.date.modifydate20230627112239-
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약학대학 > 약학과 > Journal papers
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