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dc.contributor.author유충규*
dc.contributor.author김화정*
dc.date.accessioned2016-08-28T11:08:18Z-
dc.date.available2016-08-28T11:08:18Z-
dc.date.issued1999*
dc.identifier.issn0960-894X*
dc.identifier.otherOAK-290*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/218556-
dc.description.abstract6-Arylamino-5,8-quinolinediones 3 and 7-arylamino-5,8-isoquinolinediones 4 were synthesized as inhibitors of endothelium-dependent vasorelaxation. The quinones inhibited the vasorelaxation of rat aorta with the endothelium. Among them, the quinones 3a, 3b, 3f, 4b, 4d and 4g strongly inhibited the vasorelaxation.*
dc.languageEnglish*
dc.title6-Arylamino-5,8-quinolinediones and 7-arylamino-5,8-isoquinolinediones as inhibitors of endothelium-dependent vasorelaxation*
dc.typeArticle*
dc.relation.issue17*
dc.relation.volume9*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage2469*
dc.relation.lastpage2472*
dc.relation.journaltitleBioorganic and Medicinal Chemistry Letters*
dc.identifier.doi10.1016/S0960-894X(99)00411-4*
dc.identifier.wosidWOS:000082476300003*
dc.identifier.scopusid2-s2.0-0033530103*
dc.author.googleRyu C.-K.*
dc.author.googleJung S.-H.*
dc.author.googleLee J.-A.*
dc.author.googleKim H.-J.*
dc.author.googleLee S.-H.*
dc.author.googleChung J.-H.*
dc.contributor.scopusid유충규(15846918400)*
dc.contributor.scopusid김화정(56670336100)*
dc.date.modifydate20240118124308*
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약학대학 > 약학과 > Journal papers
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