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dc.contributor.author박혜영*
dc.contributor.author김화정*
dc.date.accessioned2016-08-28T12:08:57Z-
dc.date.available2016-08-28T12:08:57Z-
dc.date.issued2010*
dc.identifier.issn0968-0896*
dc.identifier.otherOAK-6366*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/220614-
dc.description.abstractA series of novel non-peptide diamide compounds was synthesized and evaluated as antibradykinin agents by utilizing guinea-pig ileum smooth muscle. Among the final compounds, (Z)-4-(4-(bis(4-fluorophenyl)methyl)piperazin-1-yl)-4-oxo-N-(4-phenylbutan-2-yl)but-2-enamide showed most favorable bradykinin inhibitory activity and demonstrated analgesic efficacies in the rat models of inflammatory and neuropathic pain. © 2010.*
dc.languageEnglish*
dc.titleSynthesis and bradykinin inhibitory activity of novel non-peptide compounds, and evaluation of in vivo analgesic activity*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume18*
dc.relation.indexSCI*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage2327*
dc.relation.lastpage2336*
dc.relation.journaltitleBioorganic and Medicinal Chemistry*
dc.identifier.doi10.1016/j.bmc.2010.01.050*
dc.identifier.wosidWOS:000275513700029*
dc.identifier.scopusid2-s2.0-77649238323*
dc.author.googleKam Y.L.*
dc.author.googleRhee H.-K.*
dc.author.googleKim H.-J.*
dc.author.googleBack S.K.*
dc.author.googleNa H.S.*
dc.author.googleChoo H.-Y.P.*
dc.contributor.scopusid박혜영(34972649500;57200273796)*
dc.contributor.scopusid김화정(56670336100)*
dc.date.modifydate20240118124308*
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약학대학 > 약학과 > Journal papers
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