2010 | A new DNA building block, 4′-selenothymidine: Synthesis and modification to 4′-seleno-AZT as a potential anti-HIV agent | 정낙신; 최원준 | Article |
2011 | A3 adenosine receptor agonist reduces brain ischemic injury and inhibits inflammatory cell migration in rats | 정낙신 | Article |
2007 | Alternative and improved syntheses of highly potent and selective A 3 adenosine receptor agonists, CI-IB-MECA and thio-CI-IB-MECA | 정낙신 | Article |
2013 | C-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor | 정낙신; 이혁우 | Article |
2006 | Conversion of A3 adenosine receptor agonists into selective antagonists by modification of the 5′-ribofuran-uronamide moiety | 정낙신 | Article |
2005 | D-4′-thioadenosine derivatives as highly potent and selective agonists at the human A3 adenosine receptor | 정낙신 | Conference Paper |
2009 | Design and synthesis of N6-substituted-4′-thioadenosine-5′-uronamides as potent and selective human A3 adenosine receptor agonists | 정낙신; 최원준 | 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 |
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 |
2005 | Development of potent and selective human A3 adenosine receptor agonists. | 정낙신; 이상국 | Article |
2012 | Fluorocyclopentenyl-cytosine with broad spectrum and potent antitumor activity | 정낙신; 최원준 | Article |
2012 | Improved synthesis of a DNA-dependent protein kinase inhibitor IC86621 | 정낙신 | Article |
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 |