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dc.contributor.author이상국-
dc.date.accessioned2017-01-05T02:01:10Z-
dc.date.available2017-01-05T02:01:10Z-
dc.date.issued2004-
dc.identifier.issn0365-6233-
dc.identifier.otherOAK-1827-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/233651-
dc.description.abstractA series of styrylquinazoline derivatives (2 a-k) were prepared and evaluated for their inhibiton of prostaglandin E2 (PGE2) production by cyclooxygenase-2 (COX-2). The latter was induced by lipopolysaccharide-stimulated macrophage cells RAW264.7. 3′,4′ -Dihydroxylated styrylquinazolines (2 a-c), 3′-hydroxylated styrylquineizolines (2h, 2i), and 3′-acetoxy-styrylquinazolines (2j, 2k) exhibited good inhibitory effects of PGE2 production by COX-2 with a range of IC50 values of 1.19 ∼ 3.56 μM. The potencies were comparable or better than that of the representative stilbene resveratrol (IC50 = 3.07 μM). These results indicate that styrylquinazolines can be considered as potential resveratrol analogues in the modulation of prostaglandin production by COX-2.-
dc.languageEnglish-
dc.titleStyrylquinazolines: A New Class of Inhibitors on Prostaglandin E 2 Production in Lipopolysaccharide-activated Macrophage Cells-
dc.typeArticle-
dc.relation.issue1-
dc.relation.volume337-
dc.relation.indexSCI-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage20-
dc.relation.lastpage24-
dc.relation.journaltitleArchiv der Pharmazie-
dc.identifier.doi10.1002/ardp.200300791-
dc.identifier.wosidWOS:000188857200003-
dc.identifier.scopusid2-s2.0-1242269414-
dc.author.googlePark J.H.-
dc.author.googleMin H.-Y.-
dc.author.googleKim S.S.-
dc.author.googleLee J.Y.-
dc.author.googleLee S.K.-
dc.author.googleLee Y.S.-
dc.contributor.scopusid이상국(36067620500)-
dc.date.modifydate20211210153309-
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약학대학 > 약학과 > Journal papers
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