| 2000 | A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents | 김길수; 정낙신 | Article |
| 2010 | A new DNA building block, 4′-selenothymidine: Synthesis and modification to 4′-seleno-AZT as a potential anti-HIV agent | 정낙신; 최원준 | Article |
| 2002 | A short and efficient synthetic approach to hydroxy (E)-stilbenoids via solid-phase cross metathesis | 정낙신 | Article |
| 2012 | A straightforward synthesis of K-7174, a GATA-specific inhibitor | 정낙신 | Article |
| 2011 | A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats | 정낙신 | Article |
| 2010 | A3 adenosine receptor antagonist, truncated thio-Cl-IB-MECA, induces apoptosis in T24 human bladder cancer cells | 정낙신; 최원준 | Article |
| 2007 | Alternative and improved syntheses of highly potent and selective A 3 adenosine receptor agonists, CI-IB-MECA and thio-CI-IB-MECA | 정낙신 | Article |
| 2007 | Asymmetric synthesis and biological activity of l-bicyclocarba-d4T | 정낙신 | Article |
| 2007 | Asymmetric synthesis of apio fluoroneplanocin a analogs as potential AdoHcy hydrolase inhibitor | 정낙신 | Article |
| 2007 | Asymmetric synthesis of cyclopropyl-fused 2′-C-methylcarbanucleosides as potential anti-HCV agents | 이강만; 이승진; 신윤용; 정낙신 | Article |
| 2006 | Asymmetric synthesis of homo-apioneplanocin A from d-ribose | 이강만; 정낙신 | Article |
| 2007 | Asymmetric synthesis of novel apio carbocyclic nucleoside analogues as potential antiviral and antitumor agent | 이강만; 정낙신 | Conference Paper |
| 2007 | Asymmetric synthesis of novel pseudo-D-vinylcyclopropyl nucleosides bearing quaternary carbon as potential anti-herpesvirus agent | 정낙신 | Article |
| 2004 | Asymmetric Synthesis of Novel Thioiso Dideoxynucleosides with Exocyclic Methylene as Potential Antiviral Agents | 정낙신 | Article |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 2007 | Design, synthesis, and anti-tumor activity of 4′-thionucleosides as potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
