Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 정낙신 | - |
dc.date.accessioned | 2017-01-18T02:01:25Z | - |
dc.date.available | 2017-01-18T02:01:25Z | - |
dc.date.issued | 2007 | - |
dc.identifier.issn | 1525-7770 | - |
dc.identifier.other | OAK-4492 | - |
dc.identifier.uri | https://dspace.ewha.ac.kr/handle/2015.oak/233916 | - |
dc.description.abstract | Several N6-substituted 3′-ureidoadenosine derivatives were efficiently synthesized starting from D-glucose for the development of H272E mutant A3 adenosine receptor (AR) agonists. Among compounds tested, 3′-ureido-N6-(3-iodobenzyl)adenosine (2c) exhibited the highest binding affinity (Ki = 0.22 μ M) at the H272E mutant A3 AR without binding to the natural A3AR. Copyright © Taylor & Francis Group, LLC. | - |
dc.language | English | - |
dc.title | Synthesis of N6-Substituted 3′-ureidoadenosine derivatives as highly potent agonists at the mutant A3 adenosine receptor | - |
dc.type | Conference Paper | - |
dc.relation.issue | 41432 | - |
dc.relation.volume | 26 | - |
dc.relation.index | SCIE | - |
dc.relation.index | SCOPUS | - |
dc.relation.startpage | 717 | - |
dc.relation.lastpage | 719 | - |
dc.relation.journaltitle | Nucleosides, Nucleotides and Nucleic Acids | - |
dc.identifier.doi | 10.1080/15257770701493161 | - |
dc.identifier.wosid | WOS:000251875300037 | - |
dc.identifier.scopusid | 2-s2.0-36949021349 | - |
dc.author.google | Jeong L.S. | - |
dc.author.google | Choe S.A. | - |
dc.author.google | Kim A.Y. | - |
dc.author.google | Kim H.O. | - |
dc.author.google | Gao Z.-G. | - |
dc.author.google | Jacobson K.A. | - |
dc.author.google | Chun M.W. | - |
dc.author.google | Moon H.R. | - |
dc.contributor.scopusid | 정낙신(16028528200) | - |
dc.date.modifydate | 20211210153610 | - |