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Showing results 1 to 30 of 130

Issue DateTitleAuthor(s)Type
20122-(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-region최선Article
20132-(3-Fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists: Structure activity relationships of the 2-oxy pyridine C-region최선Article
20212-(Halogenated Phenyl) acetamides and propanamides as potent TRPV1 antagonists최선Article
20142-Alkyl/alkenyl substituted pyridine C-region analogues of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists최선Article
20142-Aryl substituted pyridine C-region analogues of 2-(3-fluoro-4- methylsulfonylaminophenyl)propanamides as highly potent TRPV1 antagonists최선Article
20162-Sulfonamidopyridine C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists최선Article
20093D-QSAR studies of cytotoxic heterocyclic quinones using calculated reduction potential박혜영; 최선Article
20083D-QSAR studies of heterocyclic quinones with inhibitory activity on vascular smooth muscle cell proliferation using pharmacophore-based alignment유충규; 최선Article
20184-Aminophenyl acetamides and propanamides as potent transient receptor potential vanilloid 1 (TRPV1) ligands최선Article
20155-Lipoxygenase inhibitors suppress RANKL-induced osteoclast formation via NFATc1 expression박혜영; 최선Article
20156,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists최선Article
20128-Hydroxy-2-deoxyguanosine prevents plaque formation and inhibits vascular smooth muscle cell activation through Rac1 inactivation하헌주; 최선; 조한중Article
2015A Facile and Efficient Synthesis of Seleno-acyclic Nucleosides as Potential Antiviral AgentsTamima UmmeMaster's Thesis
2016A novel pyrazole derivative protects from ovariectomy-induced osteoporosis through the inhibition of NADPH oxidase배윤수; 이수영; 이화정; 최선Article
2018Adaptable Small Ligand of CYP1 Enzymes for Use in Understanding the Structural Features Determining Isoform Selectivity최선; 이윤지Article
2020Advances in Molecular Dynamics Simulations and Enhanced Sampling Methods for the Study of Protein Systems최선; Siti Raudah Mohamed LazimReview
2007alpha-Substituted N-(4-t-butylbenzyl)-N'-[4-(methylsulfonylamino)benzyl]thiourea analogues as potent and stereospecific TRPV1 antagonists최선Meeting Abstract
2015Anti-angiogenic activity of thienopyridine derivative LCB03-0110 by targeting VEGFR-2 and JAK/STAT3 Signalling최선Article
2014Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligands최선Article
2020Asymmetric Total Syntheses of Kopsane Alkaloids via a PtCl2-Catalyzed Intramolecular [3+2] Cycloaddition최선Article
2020Asymmetric Total Syntheses of Kopsane Alkaloids via a PtCl2-Catalyzed Intramolecular [3+2] Cycloaddition최선Article
2006Balancing focused combinatorial libraries based on multiple GPCR ligands최선Article
2022Big data and artificial intelligence (AI) methodologies for computer-aided drug design (CADD)최선Review
2007Binding mode analysis of topoisomerase inhibitors, 6-arylamino-7-chloro- quinazoline-5,8-diones, within the cleavable complex of human topoisomerase I and DNA김춘미; 최선Article
2008Capsiate, a nonpungent capsaicin-like compound, inhibits angiogenesis and vascular permeability via a direct inhibition of Src kinase activity최선Article
2015Communication over the Network of Binary Switches Regulates the Activation of A(2A) Adenosine Receptor최선Article
2017Comprehensive computational study of glutaminyl cyclase inhibitors, TRPV1 antagonists, and cytochrome P450 inhibitorsCUI MINGHUADoctoral Thesis
2019Comprehensive mechanistic studies of a tetraspanin arginine sensor, polypharmacological profiling of montelukast, and in silico design of elongation factor 1-alpha inhibitorsMACALINO, STEPHANI JOY YARCIADoctoral Thesis
2014Design, Stereoselective Synthesis, and Biological Activity of Neplanocin A Analogues문양원Master's Thesis
2016Design, synthesis, and anticancer activity of C8-substituted-4 '-thionucleosides as potential HSP90 inhibitors최선Article

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