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dc.contributor.author이강만-
dc.contributor.author정낙신-
dc.date.accessioned2018-06-02T08:13:52Z-
dc.date.available2018-06-02T08:13:52Z-
dc.date.issued2005-
dc.identifier.issn1746-8272-
dc.identifier.otherOAK-17912-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/243903-
dc.description.abstractFor the purpose of developing optimal neoceptor-neoagonist pair, 3'-ureidoadenosine derivatives were synthesized. Among compounds tested, 2-chloro-3'-ureido-N6-(3-iodobenzyl)adenosine (10b) showed the best binding affinity (Ki = 0.20 microM) at the H272E mutant A3 AR, but was inactive at the natural A3 AR.-
dc.languageEnglish-
dc.titleSynthesis of 3'-ureidoadenosines and their high binding affinity at the mutant A3 adenosine receptor.-
dc.typeArticle-
dc.relation.issue49-
dc.relation.indexSCOPUS-
dc.relation.startpage105-
dc.relation.lastpage106-
dc.relation.journaltitleNucleic acids symposium series (2004)-
dc.identifier.scopusid2-s2.0-39049175931-
dc.author.googleKim A.Y.-
dc.author.googleKim H.O.-
dc.author.googleKim M.J.-
dc.author.googleChun M.W.-
dc.author.googleLee K.M.-
dc.author.googleJacobson K.A.-
dc.author.googleJeong L.S.-
dc.contributor.scopusid이강만(7501506362)-
dc.contributor.scopusid정낙신(16028528200)-
dc.date.modifydate20211210153610-
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약학대학 > 약학과 > Journal papers
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