| 2018 | Potent human glutaminyl cyclase inhibitors as potential anti-Alzheimer's agents: Structure-activity relationship study of Arg-mimetic region | 최선 | Article |
| 2014 | Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels | 최선 | Article |
| 2017 | Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists | 최선 | Article |
| 2018 | Recent Advances in Structure-Based Drug Design Targeting Class A G Protein-Coupled Receptors Utilizing Crystal Structures and Computational Simulations | 최선; 이윤지 | Article |
| 2021 | Recent applications of deep learning methods on evolutionand contact-based protein structure prediction | 최선 | Review |
| 2011 | Receptor activity and conformational analysis of 5′-halogenated resiniferatoxin analogs as TRPV1 ligands | 최선 | Article |
| 2015 | Role of computer-aided drug design in modern drug discovery | 최선 | Review |
| 2012 | Selectivity Enhancement Arising from Interactions at the PI3K Unique Pocket | 최선; 이정현 | Article |
| 2006 | Stereoselective functionalization of the 1′-position of 4′-thionucleosides | 정낙신; 최선; 류재상 | Article |
| 2014 | Stereoselective Synthesis and Antiviral Activity of Selenonucleosides | 안지윤 | Master's Thesis |
| 2008 | Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides | 정낙신; 최선; 최원준 | Article |
| 2018 | Structural and Biochemical Characterization of the Curcumin-Reducing Activity of CurA from Vibrio vulnificus | 최선; 박진병; 남상집; 차선신 | Article |
| 2014 | Structural basis of the phosphorylation dependent complex formation of neurodegenerative disease protein Ataxin-1 and RBM17 | 최선 | Article |
| 2021 | Structural Characterization of Receptor-Receptor Interactions in the Allosteric Modulation of G Protein-Coupled Receptor (GPCR) Dimers | 최선; Siti Raudah Mohamed Lazim | Review |
| 2011 | Structural insights into transient receptor potential vanilloid type 1 (TRPV1) from homology modeling, flexible docking, and mutational studies | 최선 | Article |
| 2011 | Structural insights into TRPV1 from homology modeling, docking, and mutational studies for the discovery of TRPV1 modulators | 최선 | Meeting Abstract |
| 2012 | Structural origins for the loss of catalytic activities of bifunctional human LTA4H revealed through molecular dynamics simulations | 최선 | Article |
| 2011 | Structural studies of S-Adenosylhomocysteine hydrolase and binding mode analysis with novel mechanism-based inhibitors, halo-neplanocin A analogs | 정낙신; 최선 | Meeting Abstract |
| 2012 | Structure activity relationships and molecular modeling of the N-(3-pivaloyloxy-2-benzylpropyl)-N '-[4-(methylsulfonylamino)benzyl] thiourea template for TRPV1 antagonism | 최선 | Meeting Abstract |
| 2015 | Structure activity relationships of benzyl C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists | 최선 | Article |
| 2018 | Structure-activity relationship investigation of Phe-Arg mimetic region of human glutaminyl cyclase inhibitors | 최선 | 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 |
| 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 |
| 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 |
| 2021 | Subtle Chemical Changes Cross the Boundary between Agonist and Antagonist: New A(3) Adenosine Receptor Homology Models and Structural Network Analysis Can Predict This Boundary | 최선; Pankaz Kumar Sharma; 이윤지 | 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 |
| 2016 | Synthesis and biological evaluation of 3-substituted 5-benzylidene-1-methyl-2-thiohydantoins as potent NADPH oxidase (NOX) inhibitors | 배윤수; 최선; 주정희 | Article |
| 2017 | Synthesis and Biological Evaluation of Novel 4’-Thio- and 4’-Selenonucleosides | Qu Shuhao | Doctoral Thesis |
| 2014 | Synthesis and Biological Evaluation of Novel 4′-Selenonucleosides | 유진하 | Doctoral Thesis |
