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dc.contributor.author류재상*
dc.date.accessioned2016-08-28T12:08:24Z-
dc.date.available2016-08-28T12:08:24Z-
dc.date.issued2011*
dc.identifier.issn0960-894X*
dc.identifier.otherOAK-7412*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/221483-
dc.description.abstractA 28-membered 1,2,3-triazolyl salicylamide library was synthesized via a Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition and evaluated for their abilities to inhibit NO production in LPS-activated RAW264.7 macrophage cells. Among 28 analogues, 29g showed a significant inhibitory activity (IC 50 = 12.8 μM). The inhibitory effects of 29g on LPS-mediated NO production in macrophage cells appeared to be associated with the suppression of iNOS expression. © 2011 Elsevier Ltd. All rights reserved.*
dc.languageEnglish*
dc.titleSyntheses of 1,2,3-triazolyl salicylamides with inhibitory activity on lipopolysaccharide-induced nitric oxide production*
dc.typeArticle*
dc.relation.issue7*
dc.relation.volume21*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1953*
dc.relation.lastpage1957*
dc.relation.journaltitleBioorganic and Medicinal Chemistry Letters*
dc.identifier.doi10.1016/j.bmcl.2011.02.034*
dc.identifier.wosidWOS:000288245100009*
dc.identifier.scopusid2-s2.0-79952489956*
dc.author.googleYoon J.*
dc.author.googleCho L.*
dc.author.googleLee S.K.*
dc.author.googleRyu J.-S.*
dc.contributor.scopusid류재상(36081118200)*
dc.date.modifydate20231120165709*
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약학대학 > 약학과 > Journal papers
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