| 2011 | Design and synthesis of 5 '-homo-4 '-fluoro-aristeromycin derivatives as potent antiviral agents | 정낙신; 최원준 | Meeting Abstract |
| 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 |
| 2011 | Design and Synthesis of Base Modified Carbanucleosides as Potential Adenosine Receptor Ligands | 김경림 | Master's Thesis |
| 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 |
| 2001 | Design and synthesis of novel fluorocyclopropanoid nucleosides | 정낙신 | Article; Proceedings Paper |
| 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 |
| 2011 | Design, Synthesis and Binding Affinity of Novel Adenosine Analogues as Potent Adenosine Receptor Ligands | Hou, Xiyan | Doctoral Thesis |
| 2011 | Design, Synthesis, and Anti-HCV Activity of 2 '-Modified-4 '-selenonucleosides | 정낙신; 최원준; 이혁우 | Meeting Abstract |
| 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 | Design, synthesis, and anticancer activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Meeting Abstract |
| 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 a multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 최선 | Meeting Abstract |
| 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 |
| 2010 | Design, Synthesis, Anti-Hepatitis C Virus (HCV) Activity of 3΄-C-Substituted Purine and Pyrimidine Nucleosides | 김유민 | Master's Thesis |
| 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 |
| 2007 | Development of novel clinical candidates targeting A(3) adenosine receptor | 정낙신 | Meeting Abstract |
| 2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
