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Showing results 1 to 30 of 90

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
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
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
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
2006Balancing focused combinatorial libraries based on multiple GPCR ligands최선Article
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
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
2010Design, synthesis, and binding of homologated truncated 4′-thioadenosine derivatives at the human A3 adenosine receptors정낙신; 최선; 최원준Article
2014Design, Synthesis, and Biological Activity of 6′-β-Fluoroaristeromycin Analogues as Potent S-Adenosylhomocysteine Hydrolase Inhibitor김상아Master's Thesis
2007Design, synthesis, and molecular modeling studies of 5'-deoxy-5'-ureidoadenosine: 5'-ureido group as a multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase이강만; 정낙신; 최선Meeting Abstract
2007Design, synthesis, and molecular modeling studies of 5′-deoxy-5′-ureidoadenosine: 5′-ureido group as multiple hydrogen bonding donor in the active site of S-adenosylhomocysteine hydrolase이강만; 정낙신; 최선Article
2010Discovery of a new human A2A adenosine receptor agonist, truncated 2-hexynyl-4′-thioadenosine정낙신; 최선Article
2009Discovery of a new template for anticancer agents: 2′-deoxy-2′- fluoro-4′-selenoarabinofuranosyl-cytosine (2′-F-4′-seleno-ara- C)정낙신; 이상국; 최선; 최원준Article
2016Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic template최선Article
2009Docking studies of Farnesiferol C onto Src tyrosine kinase and focal adhesion kinase and 3D-QSAR studies of heterocyclic quinones with inhibitory activity on vascular smooth muscle cell proliferation이윤지Master's Thesis
2006Efficient synthesis of 2-substituted 2,3-dihydro-4-quinolones as potential intermediates for 2-substituted 1,2,3,4-tetrahydro-4-quinolone antitumor agents최선; 류재상Article
2008FAK/SRC PATHWAY PLAYS A KEY ROLE IN FARNESIFEROL C INDUCED ANTIANGIOGENIC AND ANTITUMOR ACTIVITIES최선; 이윤지Meeting Abstract
2016Harnessing the Therapeutic Potential of Capsaicin and Its Analogues in Pain and Other Diseases최선Review

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