| 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 |
| 2003 | Design, synthesis, and in vitro evaluation of APIO analogue of neplanocin A | 정낙신 | Conference Paper |
| 2007 | Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 최선 | Article |
| 2009 | Design, synthesis, antitumor activity and mode of action of novel oxiranyl and thiiranyl phenol derivatives | 정낙신 | Article |
| 2008 | Development of A3 adenosine receptor ligands. | 정낙신 | Article |
| 2009 | Development of next generation 4'-selenonucleosides. | 정낙신 | Article |
| 2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
| 2010 | Discovery of a new human A2A adenosine receptor agonist, truncated 2-hexynyl-4′-thioadenosine | 정낙신; 최선 | Article |
| 2006 | Docking studies of agonists and antagonists suggest an activation pathway of the A3 adenosine receptor | 정낙신 | Article |
| 2021 | Dual actions of a2a and a3 adenosine receptor ligand prevents obstruction-induced kidney fibrosis in mice | 하헌주 | Article |
| 2009 | Efficient and practical synthesis of l-hamamelose | 정낙신 | Article |
| 2006 | Establishment of an assay for P2X7 receptor-mediated cell death | 정낙신 | Article |
| 2010 | First synthesis of 2′-oxabicyclo[3.1.0]hexyl nucleosides with a north conformation | 정낙신 | Article |
| 2012 | Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity | 정낙신; 최원준 | Article |
| 2009 | Highly concise synthesis of 3'-"up"-ethynyl-5'-methylbicyclo- [3.1.0]hexyl purine and pyrimidine nucleoside derivatives using rhodium(II) carbenoid cycloaddition and highly diastereoselective Grignard reaction | 정낙신 | Article |
| 2002 | Improved and alternative synthesis of D- and L-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides | 정낙신 | Article |
| 2012 | Improved synthesis of a DNA-dependent protein kinase inhibitor IC86621 | 정낙신 | Article |
| 2012 | Inactivation of the Cullin (CUL)-RING E3 ligase by the NEDD8-activating enzyme inhibitor MLN4924 triggers protective autophagy in cancer cells | 정낙신 | Short Survey |
| 2001 | Induction of Quinone Reductase Activity by Stilbene Analogs in Mouse Hepa 1c1c7 Cells | 정낙신; 이상국 | Article |
| 2008 | Inhibition of cell proliferation through cell cycle arrest and apoptosis by thio-Cl-IB-MECA, a novel A3 adenosine receptor agonist, in human lung cancer cells | 정낙신; 이상국 | Article |
| 2011 | Link between allosteric signal transduction and functional dynamics in a multisubunit enzyme: S-adenosylhomocysteine hydrolase | 정낙신; 최선 | Article |
| 2013 | Metabolism, mechanism of action and sensitivity profile of fluorocyclopentenylcytosine (RX-3117; TV-1360) | 정낙신 | Article |
| 2017 | N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation | 최선 | Article |
| 2003 | N6-substituted D-4′-thioadenosine-5′-methyluronamides: Potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Article |
| 2013 | Neddylation pathway regulates the proliferation and survival of macrophages | 정낙신 | Article |
| 2013 | New RNA purine building blocks, 4'-selenopurine nucleosides: First synthesis and unusual mixture of sugar puckerings | 정낙신; 최원준 | Article |
