| 2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
| 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 |
| 2004 | Synthesis of 5′-substituted fluoro-neplanocin A analogues: Importance of a hydrogen bonding donor at 5′-position for the inhibitory activity of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2006 | Structure-activity relationships of 2-chloro-N6-substituted- 4′-thioadenosine-5′-uronamides as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신; 이상국 | Article |
| 2007 | Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Conference Paper |
| 2003 | Design, synthesis, and biological evaluation of fluoroneplanocin A as the novel mechanism-based inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Article |
| 2006 | Design, synthesis, and biological activity of N6-substituted-4′-thioadenosines at the human A3 adenosine receptor | 정낙신; 이상국 | 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 |
| 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 |
| 2001 | Induction of Quinone Reductase Activity by Stilbene Analogs in Mouse Hepa 1c1c7 Cells | 정낙신; 이상국 | Article |
