| 2011 | Structure tuning of pyrazolylpyrrole derivatives as ERK inhibitors utilizing dual tools; 3D-QSAR and side-chain hopping | 류재상 | Article |
| 2022 | Structure, Function, and Inhibitors of the Mitochondrial Chaperone TRAP1 | 강수성 | Review |
| 2018 | Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitors | 최선 | Article |
| 2005 | Structure-activity relationship of 5′-substituted fluoro-neplanocin A analogues as potent inhibitors of S-adenosylhomocysteine hydrolase | 이강만; 정낙신; 이상국 | Conference Paper |
| 2004 | Structure-activity relationship of N6-substituted D-4 '-thioadenosine derivatives as potent and selective agonists at the human A3 adenosine receptor. | 정낙신 | Meeting Abstract |
| 2023 | Structure-Activity Relationship of Truncated 2,8-Disubstituted-Adenosine Derivatives as Dual A<sub>2A</sub>/A<sub>3</sub> Adenosine Receptor Antagonists and Their Cancer Immunotherapeutic Activity | 유진하 | Article |
| 2012 | Structure-activity relationships and molecular modeling of the N-(3-pivaloyloxy-2-benzylpropyl)-N′-[4-(methylsulfonylamino)benzyl] thiourea template for TRPV1 antagonism | 최선 | Article |
| 2007 | Structure-activity relationships of 2-chloro-N-6-substituted-4 '-thioadenosine-5 ''-dialkylamides as potent and selective human A(3) adenosine receptor antagonists | 정낙신 | Meeting Abstract |
| 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 |
| 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 |
| 2015 | Structure-Activity Relationships of Neplanocin A Analogues as S-Adenosylhomocysteine Hydrolase Inhibitors and Their Antiviral and Antitumor Activities | 창동신; 최선 | 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 |
| 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 |
| 2015 | Structure-Based Design of Bacterial Nitric Oxide Synthase Inhibitors | 강수성 | Article |
| 2007 | Structure-based inference of molecular functions of proteins of unknown function from Berkeley Structural Genomics Center | 신동해 | Review |
