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Showing results 22 to 51 of 219

Issue DateTitleAuthor(s)Type
2013C-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor정낙신; 이혁우Article
1998Carbocyclic analogues of the potent cytidine deaminase inhibitor 1-(β- D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine)정낙신Article
1997Conformational analysis of the complete series of 2' and 3' monofluorinated dideoxyuridines정낙신Article
2006Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety정낙신Article
2005D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor정낙신Conference Paper
2012Decreased expression of synapse-related genes and loss of synapses in major depressive disorder정낙신Article
2011Design and Stereoselective Synthesis of 3'-Aminoadenosine Derivatives as Potential A3 Adenosine Receptor Antagonists최문주Master's Thesis
2011Design and Synthesis of 2΄-Azido-2΄-deoxy-4΄-selenofuranosyl Pyrimidines As Potential Antiviral Agents최정희Master's Thesis
2004Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor정낙신Article
2011Design and synthesis of 5 '-homo-4 '-fluoro-aristeromycin derivatives as potent antiviral agents정낙신; 최원준Meeting Abstract
2008Design and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor정낙신Article
2003Design and synthesis of A3 adenosine receptor ligands, 2′-fluoro analogues of Cl-IB-MECA정낙신Conference Paper
2003Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA정낙신Conference Paper
2011Design and Synthesis of Base Modified Carbanucleosides as Potential Adenosine Receptor Ligands김경림Master's Thesis
2009Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists정낙신; 최원준Article
2008Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents정낙신; 최원준Article
2001Design and synthesis of novel fluorocyclopropanoid nucleosides정낙신Article; Proceedings Paper
2008Design and synthesis of truncated 4'-thioadenosine derivatives as potent and selective A3 adenosine receptor antagonists.정낙신; 최원준Article
2007Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine정낙신Article
2011Design, synthesis and anticancer activity of novel dihydrobenzofuro[4,5-b] [1,8]naphthyridin-6-one derivatives정낙신Article
2003Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands이승진; 정낙신Article
2011Design, Synthesis and Binding Affinity of Novel Adenosine Analogues as Potent Adenosine Receptor LigandsHou, XiyanDoctoral Thesis
2011Design, Synthesis, and Anti-HCV Activity of 2 '-Modified-4 '-selenonucleosides정낙신; 최원준; 이혁우Meeting Abstract
2007Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor정낙신; 이상국Article
2007Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines정낙신; 이상국Meeting Abstract
2005Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines.이강만; 정낙신; 이상국; 최원준Article
2010Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors정낙신; 최선; 최원준Article
2006Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor정낙신; 이상국Article
2003Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase이강만; 정낙신; 이상국Article
2007Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives정낙신Article