| 2005 | Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as human A3 adenosine receptor agonists | 정낙신; 이상국 | Meeting Abstract |
| 2008 | Structure-activity relationships of 2-chloro-N6-substituted-4′-thioadenosine-5′-N,N-dialkyluronamides as human A3 adenosine receptor antagonists | 정낙신; 최원준 | Article |
| 2014 | Structure-activity relationships of 2′-modified-4′- selenoarabinofuranosyl-pyrimidines as anticancer agents | 정낙신 | Article |
| 2001 | Structure-activity relationships of apio nucleosides as potential antiviral agents | 정낙신 | Conference Paper |
| 2009 | Structure-activity relationships of truncated adenosine derivatives as highly potent and selective human A3 adenosine receptor antagonists | 정낙신; 이상국; 최원준 | Article |
| 2012 | Structure-activity relationships of truncated C2- or C8-substituted adenosine derivatives as dual acting A 2A and A 3 adenosine receptor ligands | 정낙신; 최선; 최원준 | Article |
| 2008 | Structure-activity relationships of truncated D- and L-4′- thioadenosine derivatives as species-independent A3 adenosine receptor antagonists | 정낙신; 이상국; 최원준 | Article |
| 2002 | Study of the stability of carbocations by chlorosulfonyl isocyanate reaction with ethers | 정낙신 | Article |
| 2011 | Suppression of inflammation response by a novel A 3 adenosine receptor agonist thio-Cl-IB-MECA through inhibition of Akt and NF-κB signaling | 정낙신; 이혁우 | Article |
| 1997 | Syntheses and antiviral activities of 1,3-dioxolanyl-, 1,3-oxathiolanyl- and 1,3-dithiolanylnucleosides with 2-hydroxymethyl substituents | 정낙신 | Article |
| 2008 | Syntheses and Biological Activity of Neplanocin and Analogues | 정낙신 | Chapter |
| 2001 | Syntheses and structure-activity relationships of novel apio and thioapio dideoxydidehydronucleosides as anti-HCMV agents | 정낙신 | Article |
| 2001 | Syntheses of D- and L-cyclopentenone derivatives using ring-closing metathesis: Versatile intermediates for the synthesis of D- and L-carbocyclic nucleosides | 정낙신 | Article |
| 2007 | Synthesis and anti-HCV activity of 2′-β-hydroxymethylated nucleosides | 이강만; 정낙신 | Conference Paper |
| 2010 | Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C- substituted-methyl pyrimidine and purine nucleosides | 정낙신; 최원준 | Article |
| 2014 | Synthesis and anti-renal fibrosis activity of conformationally locked truncated 2-hexynyl-N6-substituted-(N)-methanocarba-nucleosides as A3 adenosine receptor antagonists and partial agonists | 정낙신; 하헌주; 최선 | Article |
| 2005 | Synthesis and anti-tumor activity of fluorocyclopentenyl-pyrimidines | 정낙신 | Meeting Abstract |
| 2008 | Synthesis and antitumor activity of 1-beta-4-selenoarabinofuranosyl cytosine (4'-seleno-ara-C). | 정낙신; 이상국; 최원준 | Article |
| 2007 | Synthesis and antitumor activity of fluorocyclopentenyl-pyrimidines | 정낙신; 이상국 | Conference Paper |
| 1999 | Synthesis and antiviral activities of 1,3-oxathiolanyl nucleosides with 5-hydroxymethyl substituent | 정낙신 | Conference Paper |
| 2001 | Synthesis and antiviral activity of 2 '-"up"-azido-2 ',3 '-dideoxy-4 '-thionucleosides. | 정낙신 | Meeting Abstract |
| 1998 | Synthesis and antiviral activity of 2′-fluorohexopyranosyl nucleosides | 정낙신 | Article |
| 1998 | Synthesis and antiviral activity of apio dideoxy nucleosides with azido or amino substituent | 정낙신 | Article |
| 2001 | Synthesis and antiviral activity of D- and L-2′-azido-2′,3′-dideoxy-4′-thiopyrimidine and purine nucleosides | 정낙신 | Conference Paper |
| 1999 | Synthesis and antiviral activity of D- and L-isodideoxy nucleosides with exocyclic methylene | 정낙신 | Conference Paper |
| 2001 | Synthesis and Antiviral Activity of Fluoro-substituted Apio Dideoxynucleosides | 정낙신 | Article |
| 1999 | Synthesis and antiviral activity of L-2'-deoxy-2'-up-fluoro-4'- thionucleosides | 정낙신 | Conference Paper |
| 2001 | Synthesis and antiviral activity of novel D- and L-2′-azido-2′,3′-dideoxyribofuranosyl-4′- thiopyrimidines and purines | 정낙신 | Article |
| 1998 | Synthesis and antiviral activity of novel isodideoxy nucleosides with exocyclic methylene | 정낙신 | Article |
| 2005 | Synthesis and binding affinity of 3'-ureidoadenosine analogues at the A3 adenosine receptor. | 정낙신 | Meeting Abstract |
