2000 | A highly efficient synthesis of L-β-2′-deoxy-4′-thio-1′-purine nucleosides as potential antiviral agents | 김길수; 정낙신 | Article |
2005 | A highly efficient synthesis of unnatural L-sugars from D-ribose | 정낙신; 최원준 | 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 |
2005 | A novel adenosine analog, thio-Cl-IB-MECA, induces G0/G 1 cell cycle arrest and apoptosis in human promyelocytic leukemia HL-60 cells | 정낙신; 이상국 | Article |
1998 | A short and efficient synthesis of L-thioarbinose derivative: A versatile synthon for the synthesis of l-2'-deoxy-2',2'-disubstituted-4'- thionucleosides | 정낙신 | 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 anti-RNA virus activity of cyclopropyl-fused 2 '-C-methyl-carbocyclic nucleosides | 정낙신; 장준 | Meeting Abstract |
2007 | Asymmetric synthesis and biological activity of l-bicyclocarba-d4T | 정낙신 | Article |
2012 | Asymmetric Synthesis of 6′-Fluoroaristeromycin Analogues as Potential S-Adenosylhomocysteine Hydrolase Inhibitor | 엄윤진 | Master's Thesis |
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 |
2007 | Asymmetric synthesis of homo-apioneplanocin A as a potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Meeting Abstract |
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 |
2001 | Asymmetric synthesis of the versatile intermediates for the synthesis of D- and L-carbocyclic nucleosides. | 정낙신 | Meeting Abstract |
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 |