| 2017 | N6-Substituted 5′-N-Methylcarbamoyl-4′-selenoadenosines as Potent and Selective A3 Adenosine Receptor Agonists with Unusual Sugar Puckering and Nucleobase Orientation | 최선 | 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 |
| 2014 | Overactivated neddylation pathway as a therapeutic target in lung cancer | 정낙신 | Article |
| 2011 | Regio- and stereoselective synthesis of truncated 3′- aminocarbanucleosides and their binding affinity at the A 3 adenosine receptor | 정낙신; 최원준 | 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 2010 | Synthesis and anti-hepatitis C virus (HCV) activity of 3′-C- substituted-methyl pyrimidine and purine nucleosides | 정낙신; 최원준 | Article |
| 2011 | Synthesis and binding affinity of homologated adenosine analogues as A3 adenosine receptor ligands | 정낙신; 최원준 | Article |
| 2000 | Synthesis of (-)-Neplanocin A Analogues as Potential Antiviral Agents | 정낙신 | Article |
| 2008 | Synthesis of 2-chloro-N6-substituted-4'-thioadenosine-5'-N, N-dialkyluronamides as potent and selective A3 adenosine receptor antagonists. | 정낙신; 최원준 | Article |
| 2005 | Synthesis of 3′-ureidoadenosine analogues and their binding affinity to the A3 adenosine receptor | 정낙신 | Conference Paper |
| 2006 | The antitumor effect of LJ-529, a novel agonist to A3 adenosine receptor, in both estrogen receptor-positive and estrogen receptor-negative human breast cancers | 정낙신 | Article |
| 2012 | The Nedd8-activating enzyme inhibitor MLN4924 induces autophagy and apoptosis to suppress liver cancer cell growth | 정낙신 | Article |
| 2013 | The selective A3AR antagonist LJ-1888 ameliorates UUO-induced tubulointerstitial fibrosis | 정낙신; 하헌주; 이정현 | Article |
| 2011 | X-ray crystal structure and binding mode analysis of human S-adenosylhomocysteine hydrolase complexed with novel mechanism-based inhibitors, haloneplanocin A analogues | 이강만; 정낙신; 최선; 최원준 | Article |
