2012 | N-4-t-Butylbenzyl 2-(4-methylsulfonylaminophenyl) propanamide TRPV1 antagonists: Structure-activity relationships in the A-region | 최선 | 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 |
2019 | Network-based integrated analysis of omics data reveal novel players of TGF-β1-induced EMT in human peritoneal mesothelial cells | 이공주; 하헌주 | Article |
2010 | New algorithm for the identification of intact disulfide linkages based on fragmentation characteristics in tandem mass spectra | 이공주 | Article |
2011 | Novel oxidative modifications in redox-active cysteine residues | 이공주; 최선; 신동해 | Article |
2006 | Nuclear factor-κB activated by capacitative Ca2+ entry enhances muscarinic receptor-mediated soluble amyloid precursor protein (sAPPα) release in SH-SY5Y cells | 김화정; 최신규 | Article |
2009 | Oxidative modifications of glyceraldehyde-3-phosphate dehydrogenase play a key role in its multiple cellular functions | 이공주; 김영미; 최선 | Article |
2006 | Phospholipase A2 is involved in muscarinic receptor-mediated sAPPα release independently of cyclooxygenase or lypoxygenase activity in SH-SY5Y cells | 김화정; 최신규 | Article |
2014 | Promiscuous gating modifiers target the voltage sensor of Kv7.2, TRPV1, and Hv1 cation channels | 최선 | Article |
2009 | Proton pump inhibitors exert anti-allergic effects by reducing TCTP secretion | 이경림; 황은숙 | Article |
2017 | Pyrazole C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists | 최선 | Article |
2003 | QSAR study of quinolinediones with inhibitory activity of endothelium-dependent vasorelaxation by CoMSIA | 유충규; 박혜영; 김화정 | 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 |
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 |
2008 | Stereoselective synthesis and conformational study of novel 2′,3′-didehydro-2′,3′-dideoxy-4′-selenonucleosides | 정낙신; 최선; 최원준 | Article |
2014 | Structural basis of the phosphorylation dependent complex formation of neurodegenerative disease protein Ataxin-1 and RBM17 | 최선 | Article |
2011 | Structural insights into transient receptor potential vanilloid type 1 (TRPV1) from homology modeling, flexible docking, and mutational studies | 최선 | Article |
2012 | Structural origins for the loss of catalytic activities of bifunctional human LTA4H revealed through molecular dynamics simulations | 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 |
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 |
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 |
2003 | The 3D-QSAR study of antitumor arylsulfonylimidazolidinone derivatives by CoMFA and CoMSIA | 박혜영 | 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 |
2011 | trans-Stilbenoids: Potent and selective inhibitors for human cytochrome P450 1B1 | 최선 | Article |