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Issue DateTitleAuthor(s)Type
2004Preparative and stereoselective synthesis of the versatile intermediate D-cyclopentenone with 4-hydroxymethyl substituent for the synthesis of carbocyclic nucleosides이강만; 정낙신Meeting Abstract
2006Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists정낙신Article
2006Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
2006Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety정낙신Article
2004Synthesis of apio analogues of neplanocin a and their inhibitory activity against S-adenosylhomocysteine hydrolase.정낙신Meeting Abstract
2010Nucleoside-derived antagonists to A3 adenosine receptors lower mouse intraocular pressure and act across species정낙신Article
2003N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor정낙신Article
2011A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats정낙신Article
2013Recent Advances in Synthesis and Biological Activity of 4'-Thionucleosides정낙신Chapter
1997Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents정낙신Article
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