DSpace at EWHA: Development of potent and selective human A3 adenosine receptor agonists.

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DC Field	Value	Language
dc.contributor.author	정낙신	-
dc.contributor.author	이상국	-
dc.date.accessioned	2018-06-02T08:13:51Z	-
dc.date.available	2018-06-02T08:13:51Z	-
dc.date.issued	2005	-
dc.identifier.issn	1746-8272	-
dc.identifier.other	OAK-17916	-
dc.identifier.uri	https://dspace.ewha.ac.kr/handle/2015.oak/243900	-
dc.description.abstract	On the basis of bioisosteric rationale, structure-activity relationship of Cl-IB-MECA, which showed high binding affinity at the human A3 adenosine receptor, was studied. From this study, 2-chloro-4'-thioadenosine-5'-methyluronamide was discovered as the most potent and selective agonist at the human A3 adenosine receptor.	-
dc.language	English	-
dc.title	Development of potent and selective human A3 adenosine receptor agonists.	-
dc.type	Article	-
dc.relation.issue	49	-
dc.relation.index	SCOPUS	-
dc.relation.startpage	31	-
dc.relation.lastpage	32	-
dc.relation.journaltitle	Nucleic acids symposium series (2004)	-
dc.identifier.scopusid	2-s2.0-39049190345	-
dc.author.google	Jeong L.S.	-
dc.author.google	Lee H.W.	-
dc.author.google	Jacobson K.A.	-
dc.author.google	Lee S.K.	-
dc.author.google	Chun M.W.	-
dc.contributor.scopusid	정낙신(16028528200)	-
dc.contributor.scopusid	이상국(36067620500)	-
dc.date.modifydate	20211210153309	-