2012 | 2-(3-Fluoro-4-methylsulfonylaminophenyl)propanamides as potent transient receptor potential vanilloid 1 (TRPV1) antagonists: Structure-activity relationships of 2-amino derivatives in the N-(6-trifluoromethylpyridin-3- ylmethyl) C-region | 최선 | Article |
2013 | 2-(3-Fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists: Structure activity relationships of the 2-oxy pyridine C-region | 최선 | Article |
2021 | 2-(Halogenated Phenyl) acetamides and propanamides as potent TRPV1 antagonists | 최선 | Article |
2014 | 2-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists | 최선 | Article |
2014 | 2-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4- methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists | 최선 | Article |
2016 | 2-Sulfonamidopyridine C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists | 최선 | Article |
2009 | 3D-QSAR studies of cytotoxic heterocyclic quinones using calculated reduction potential | 박혜영; 최선 | Article |
2008 | 3D-QSAR studies of heterocyclic quinones with inhibitory activity on vascular smooth muscle cell proliferation using pharmacophore-based alignment | 유충규; 최선 | Article |
2018 | 4-Aminophenyl acetamides and propanamides as potent transient receptor potential vanilloid 1 (TRPV1) ligands | 최선 | Article |
2015 | 5-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression | 박혜영; 최선 | Article |
2015 | 6,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists | 최선 | Article |
2012 | 8-Hydroxy-2-deoxyguanosine prevents plaque formation and inhibits vascular smooth muscle cell activation through Rac1 inactivation | 하헌주; 최선; 조한중 | Article |
2015 | A Facile and Efficient Synthesis of Seleno-acyclic Nucleosides as Potential Antiviral Agents | Tamima Umme | Master's Thesis |
2016 | A novel pyrazole derivative protects from ovariectomy-induced osteoporosis through the inhibition of NADPH oxidase | 배윤수; 이수영; 이화정; 최선 | Article |
2018 | Adaptable Small Ligand of CYP1 Enzymes for Use in Understanding the Structural Features Determining Isoform Selectivity | 최선; 이윤지 | Article |
2020 | Advances in Molecular Dynamics Simulations and Enhanced Sampling Methods for the Study of Protein Systems | 최선; Siti Raudah Mohamed Lazim | Review |
2023 | Albumin-binding photosensitizer capable of targeting glioma via the SPARC pathway | 최선 | Article |
2007 | alpha-Substituted N-(4-t-butylbenzyl)-N'-[4-(methylsulfonylamino)benzyl]thiourea analogues as potent and stereospecific TRPV1 antagonists | 최선 | Meeting Abstract |
2015 | Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 Signalling | 최선 | Article |
2014 | Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligands | 최선 | Article |
2020 | Asymmetric Total Syntheses of Kopsane Alkaloids via a PtCl2-Catalyzed Intramolecular [3+2] Cycloaddition | 최선 | Article |
2020 | Asymmetric Total Syntheses of Kopsane Alkaloids via a PtCl2-Catalyzed Intramolecular [3+2] Cycloaddition | 최선 | Article |
2006 | Balancing focused combinatorial libraries based on multiple GPCR ligands | 최선 | Article |
2022 | Big data and artificial intelligence (AI) methodologies for computer-aided drug design (CADD) | 최선 | Review |
2007 | Binding mode analysis of topoisomerase inhibitors, 6-arylamino-7-chloro- quinazoline-5,8-diones, within the cleavable complex of human topoisomerase I and DNA | 김춘미; 최선 | Article |
2008 | Capsiate, a nonpungent capsaicin-like compound, inhibits angiogenesis and vascular permeability via a direct inhibition of Src kinase activity | 최선 | Article |
2022 | CHARMM-GUI Enhanced Sampler for various collective variables and enhanced sampling methods | 최선 | Article |
2015 | Communication over the Network of Binary Switches Regulates the Activation of A(2A) Adenosine Receptor | 최선 | Article |
2017 | Comprehensive computational study of glutaminyl cyclase inhibitors, TRPV1 antagonists, and cytochrome P450 inhibitors | CUI MINGHUA | Doctoral Thesis |
2019 | Comprehensive mechanistic studies of a tetraspanin arginine sensor, polypharmacological profiling of montelukast, and in silico design of elongation factor 1-alpha inhibitors | MACALINO, STEPHANI JOY YARCIA | Doctoral Thesis |