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dc.contributor.author정낙신-
dc.date.accessioned2016-08-29T12:08:17Z-
dc.date.available2016-08-29T12:08:17Z-
dc.date.issued2008-
dc.identifier.issn1746-8272-
dc.identifier.otherOAK-18111-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/231236-
dc.description.abstract4'-Thioadenosines have been discovered as novel templates for A(3) adenosine ligands. Among these, 4'-thioadenosine-5'-monoalkyluronamides were discovered as novel potent and selective A(3) adenosine receptor agonists, while 4'-thioadenosine-5'-dialkyluronamides and truncated 4'-thioadenosine derivatives exhibited potent and selective antagonism at the A(3) adenosine receptor.-
dc.languageEnglish-
dc.titleDevelopment of A3 adenosine receptor ligands.-
dc.typeArticle-
dc.relation.issue52-
dc.relation.indexSCOPUS-
dc.relation.startpage79-
dc.relation.lastpage80-
dc.relation.journaltitleNucleic acids symposium series (2004)-
dc.identifier.scopusid2-s2.0-78649424920-
dc.author.googleJeong L.S.-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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