2013 | C-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor | 정낙신; 이혁우 | Article |
1998 | Carbocyclic analogues of the potent cytidine deaminase inhibitor 1-(β- D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) | 정낙신 | Article |
1997 | Conformational analysis of the complete series of 2' and 3' monofluorinated dideoxyuridines | 정낙신 | Article |
2006 | Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety | 정낙신 | Article |
2005 | D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Conference Paper |
2012 | Decreased expression of synapse-related genes and loss of synapses in major depressive disorder | 정낙신 | Article |
2011 | Design and Stereoselective Synthesis of 3'-Aminoadenosine Derivatives as Potential A3 Adenosine Receptor Antagonists | 최문주 | Master's Thesis |
2011 | Design and Synthesis of 2΄-Azido-2΄-deoxy-4΄-selenofuranosyl Pyrimidines As Potential Antiviral Agents | 최정희 | Master's Thesis |
2004 | Design and synthesis of 3′-ureidoadenosine-5′-uronamides: Effects of the 3′-ureido group on binding to the A 3 adenosine receptor | 정낙신 | Article |
2011 | Design and synthesis of 5 '-homo-4 '-fluoro-aristeromycin derivatives as potent antiviral agents | 정낙신; 최원준 | Meeting Abstract |
2008 | Design and synthesis of 5''-iodoneplanocin a and its analogues as potential S-adenosylhomocysteine hydrolase inhibitor | 정낙신 | Article |
2003 | Design and synthesis of A3 adenosine receptor ligands, 2′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
2003 | Design and synthesis of A3 adenosine receptor ligands, 3′-fluoro analogues of Cl-IB-MECA | 정낙신 | Conference Paper |
2011 | Design and Synthesis of Base Modified Carbanucleosides as Potential Adenosine Receptor Ligands | 김경림 | Master's Thesis |
2009 | Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists | 정낙신; 최원준 | Article |
2008 | Design and synthesis of novel 2′,3′-dideoxy-4′-selenonucleosides as potential antiviral agents | 정낙신; 최원준 | Article |
2001 | Design and synthesis of novel fluorocyclopropanoid nucleosides | 정낙신 | Article; Proceedings Paper |
2008 | Design and synthesis of truncated 4'-thioadenosine derivatives as potent and selective A3 adenosine receptor antagonists. | 정낙신; 최원준 | Article |
2007 | Design, enantiopure synthesis, and biological evaluation of novel ISO-D-2′,3′-dideoxy-3′-fluorothianucleoside derivatives as a bioisostere of lamivudine | 정낙신 | Article |
2011 | Design, synthesis and anticancer activity of novel dihydrobenzofuro[4,5-b] [1,8]naphthyridin-6-one derivatives | 정낙신 | Article |
2003 | Design, synthesis and binding affinity of 3′-fluoro analogues of Cl-IB-MECA as adenosine A3 receptor ligands | 이승진; 정낙신 | Article |
2011 | Design, Synthesis and Binding Affinity of Novel Adenosine Analogues as Potent Adenosine Receptor Ligands | Hou, Xiyan | Doctoral Thesis |
2011 | Design, Synthesis, and Anti-HCV Activity of 2 '-Modified-4 '-selenonucleosides | 정낙신; 최원준; 이혁우 | Meeting Abstract |
2007 | Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
2007 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Meeting Abstract |
2005 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines. | 이강만; 정낙신; 이상국; 최원준 | Article |
2010 | Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors | 정낙신; 최선; 최원준 | Article |
2006 | Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
2007 | Design, synthesis, and biological evaluation of novel iso-d-2′,3′-dideoxy-3′-fluorothianucleoside derivatives | 정낙신 | Article |