| 2010 | Discovery of a new human A2A adenosine receptor agonist, truncated 2-hexynyl-4′-thioadenosine | 정낙신; 최선 | Article |
| 2007 | Discovery of a new nucleoside template for human A3 adenosine receptor ligands: D-4′-thioadenosine derivatives without 4′-hydroxymethyl group as highly potent and selective antagonists | 정낙신; 이상국 | Article |
| 2009 | Discovery of a new template for anticancer agents: 2′-deoxy-2′- fluoro-4′-selenoarabinofuranosyl-cytosine (2′-F-4′-seleno-ara- C) | 정낙신; 이상국; 최선; 최원준 | Article |
| 2006 | Docking studies of agonists and antagonists suggest an activation pathway of the A3 adenosine receptor | 정낙신 | 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 |
| 2008 | First synthesis of 4′-selenonucleosides showing unusual southern conformation | 정낙신; 이상국; 권영주 | 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 |
| 2001 | Lamivudine production via enantioselective deamination by thermostable Bacillus caldolyticus cytidine deaminase | 정낙신 | 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 |
| 2005 | Molecular recognition of 3 '-modified adenosine neoligands to the human A3 adenosine receptor and its neoceptor. | 정낙신 | Meeting Abstract |
| 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 |
| 2001 | Novel nucleosides with vinyl fluoride or vinyl bromide moiety as open-chain analogs of neplanocin A | 정낙신 | Article; Proceedings Paper |
| 2006 | Nucleoside prodrugs of A3 adenosine receptor agonists and antagonists | 정낙신 | Article |
| 2009 | Nucleoside-based adenosine A3 receptor antagonists as drug candidates | 정낙신 | Review |
| 2010 | Nucleoside-derived antagonists to A3 adenosine receptors lower mouse intraocular pressure and act across species | 정낙신 | Article |
| 2006 | Orthogonal activation of the reengineered A3 adenosine receptor (neoceptor) using tailored nucleoside agonists | 정낙신 | Article |
| 2014 | Overactivated neddylation pathway as a therapeutic target in lung cancer | 정낙신 | Article |
| 1998 | Participation of sulfur occurred during the Mitsunobu reaction: Synthesis of novel isodideoxythionucleosides | 정낙신 | Article |
| 2004 | Preparative and stereoselective synthesis of the versatile intermediate D-cyclopentenone with 4-hydroxymethyl substituent for the synthesis of carbocyclic nucleosides | 이강만; 정낙신 | Meeting Abstract |
