| 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 |
| 2017 | t-Butyl pyridine and phenyl C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists | 최선 | Article |
| 2013 | The carbonate analogues of 5 '-halogenated resiniferatoxin as TRPV1 ligands | 최선 | Article |
| 2015 | The Cell Shape-determining Csd6 Protein from Helicobacter pylori Constitutes a New Family of L,D-Carboxypeptidase | 최선; 유자경 | Article |
| 2016 | The discovery of 2,5-isomers of triazole-pyrrolopyrimidine as selective Janus kinase 2 (JAK2) inhibitors versus JAK1 and JAK3 | 최선 | Article |
| 2006 | The effects of biasing torsional mutations in a conformational GA | 최선 | Article |
| 2019 | Total Synthesis of Hoiamide A Using an Evans-Tishchenko Reaction as a Key Step | 최선 | Article |
| 2015 | Total synthesis of the putative structure of the proposed Banyasin A | 최선 | Article |
| 2022 | Total synthesis of thioamycolamide A using diastereoselective sulfa-Michael addition as the key step | 최선; Pratanphorn Nakliang | Article |
| 2011 | trans-Stilbenoids: Potent and selective inhibitors for human cytochrome P450 1B1 | 최선 | Article |
| 2015 | Transient receptor potential vanilloid type 1 antagonists: a patent review (2011-2014) | 최선; Pankaz Kumar Sharma | Review |
| 2019 | Transmembrane 4 L Six Family Member 5 Senses Arginine for mTORC1 Signaling | 최선 | Article |
| 2013 | TRPV1 antagonist with high analgesic efficacy: 2-Thio pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides | 최선 | Article |
| 2016 | Ultraslow Water-Mediated Transmembrane Interactions Regulate the Activation of A(2A) Adenosine Receptor | 최선; 이윤지 | Article |
| 2018 | Understanding G protein-coupled receptor allostery via molecular dynamics simulations: Implications for drug discovery | 최선; 이윤지 | Book Chapter |
| 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 |
| 2015 | α-Substituted 2-(3-fluoro-4-methylsulfonamidophenyl)acetamides as potent TRPV1 antagonists | 최선 | Article |
| 2007 | α-Substituted N-(4-tert-butylbenzyl)-N′-[4-(methylsulfonylamino)benzyl]thiourea analogues as potent and stereospecific TRPV1 antagonists | 최선 | Article |
