| 2008 | Selective A3 adenosine receptor antagonists derived from nucleosides containing a bicyclo[3.1.0]hexane ring system | 정낙신 | Article |
| 2019 | Small-molecule inhibitor of HlyU attenuates virulence of Vibrio species | 김병식 | Article |
| 2011 | Stereoselective amination of chiral benzylic ethers using chlorosulfonyl isocyanate: Total synthesis of (+)-Sertraline | 정낙신 | Article |
| 2012 | Stereoselective synthesis and anti-HCV activity of conformationally restricted 2′-C-substituted carbanucleosides | 정낙신; 최원준 | Article |
| 2007 | Stereoselective synthesis of 1′-functionalized-4′- thionucleosides | 정낙신 | Article |
| 2005 | Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides | 이강만; 신윤용; 정낙신 | Conference Paper |
| 2002 | Stereoselective synthesis of a novel apio analogue of neplanocin A as potential S-adenosylhomocysteine hydrolase inhibitor | 이강만; 정낙신 | Article |
| 2002 | Stereoselective synthesis of amino-substituted apio dideoxynucleosides through a distant neighboring group effect | 정낙신 | Article |
| 2005 | Stereoselective synthesis of conformationally rigid apio carbanucleosides as potential antiviral agents | 정낙신 | Conference Paper |
| 2012 | Stereoselective synthesis of fluoro-homoneplanocin A as a potential antiviral agent | 정낙신 | Article |
| 2007 | Stereoselective synthesis of homo-apioneplanocin A as potential inhibitor of S-adenosylhomocysteine hydrolase | 이강만; 정낙신 | Conference Paper |
| 2011 | Stereoselective synthesis of MLN4924, an inhibitor of NEDD8-activating enzyme | 정낙신; 최원준 | Article |
| 2005 | Stereoselective synthesis of novel thioiso dideoxy nucleosides with exocyclic methylene as potential antiviral agents | 정낙신 | Conference Paper |
| 2004 | Structural determinants of efficacy at A3 adenosine receptors: Modification of the ribose moiety | 정낙신 | Article |
| 2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
| 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 |
| 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 |
| 2023 | Structure-Activity Relationships of Truncated 1′-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs | 최선 | Article |
| 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 |
| 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 |
| 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 |
| 2008 | Synthesis and antitumor activity of 1-beta-4-selenoarabinofuranosyl cytosine (4'-seleno-ara-C). | 정낙신; 이상국; 최원준 | Article |
