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14 articles for S Yoon


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Discovery of N-(3-fluoro-4-methylsulfonamidomethylphenyl)urea as a potent TRPV1 antagonistic template.EBI
Seoul National University
2-Sulfonamidopyridine C-region analogs of 2-(3-fluoro-4-methylsulfonamidophenyl)propanamides as potent TRPV1 antagonists.EBI
Seoul National University
Pyridine C-region analogs of 2-(3-fluoro-4-methylsulfonylaminophenyl)propanamides as potent TRPV1 antagonists.EBI
Seoul National University
6,6-Fused heterocyclic ureas as highly potent TRPV1 antagonists.EBI
Shenyang Pharmaceutical University
Design and synthesis of protein kinase C epsilon selective diacylglycerol lactones (DAG-lactones).EBI
Seoul National University
Asymmetric synthesis and receptor activity of chiral simplified resiniferatoxin (sRTX) analogues as transient receptor potential vanilloid 1 (TRPV1) ligands.EBI
Seoul National University
Identification of (beta-carboxyethyl)-rhodanine derivatives exhibiting peroxisome proliferator-activated receptor gamma activity.EBI
Sookmyung Women'S University
1,3-Diphenyl-1H-pyrazole derivatives as a new series of potent PPAR¿ partial agonists.EBI
Sookmyung Women'S University
Structure-Activity Relationships of Truncated 1'-Homologated Carbaadenosine Derivatives as New PPARγ/δ Ligands: A Study on Sugar Puckering Affecting Binding to PPARs.EBI
Seoul National University
2-(Halogenated Phenyl) acetamides and propanamides as potent TRPV1 antagonists.EBI
Seoul National University
Discovery of Leucyladenylate Sulfamates as Novel Leucyl-tRNA Synthetase (LRS)-Targeted Mammalian Target of Rapamycin Complex 1 (mTORC1) Inhibitors.EBI
Seoul National University
Discovery of an Orally Bioavailable Gonadotropin-Releasing Hormone Receptor Antagonist.EBI
Sk Chemicals
Synthesis of cinnamic amide derivatives and their anti-melanogenic effect in α-MSH-stimulated B16F10 melanoma cells.EBI
Pusan National University
Discovery of simplified leucyladenylate sulfamates as novel leucyl-tRNA synthetase (LRS)-targeted mammalian target of rapamycin complex 1 (mTORC1) inhibitors.EBI
Seoul National University