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FCC
EWHA WOMANS UNIVERSITY
COLLEGE OF PHARMACY
FIBROSIS CONTROL CENTER
논문
ewhamrc
2018-09-23T22:54:44+09:00
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[2021]
[권영주] 4-Flourophenyl-substituted 5H-indeno[1,2-b]pyridinols with enhanced topoisomerase IIα inhibitory activity: Synthesis, biological evaluation, and structure-activity relationships
[2021]
[강수성/최선] Discovery and Biological Evaluation of N-Methyl-pyrrolo[2,3- b]pyridine-5-carboxamide Derivatives as JAK1-Selective Inhibitors
[2022]
[강수성] Triphenylphosphonium conjugation to a TRAP1 inhibitor, 2-amino-6-chloro-7,9-dihydro-8H-purin-8-one increases antiproliferative activity
[2022]
[강수성] Palladium-Catalyzed α-Arylation of Cyclic β-Dicarbonyl Compounds for the Synthesis of CaV1.3 Inhibitors
[2020]
[강수성] Discovery of 2-((4-Resorcinolyl)-5-aryl-1,2,3-triazol-1-yl)acetates as potent Hsp90 inhibitors with selectivity over TRAP1
[2020]
[강수성] Development of pyrazolo[3,4-d]pyrimidine-6-amine-based TRAP1 inhibitors that demonstrate in vivo anticancer activity in mouse xenograft models
[2021]
[강수성] Design and Synthesis of TRAP1 Selective Inhibitors: H-Bonding with Asn171 Residue in TRAP1 Increases Paralog Selectivity
[2018]
[강수성] Convenient metal-free direct oxidative amidation of aldehyde using dibromoisocyanuric acid under mild conditions
[2018]
[강수성] CF3-Substituted Mollugin 2-(4-Morpholinyl)-ethyl ester as a Potential Anti-inflammatory Agent with Improved Aqueous Solubility and Metabolic Stability
[2020]
[강수성] A Single Amino Acid Determines the Selectivity and Efficacy of Selective Negative Allosteric Modulators of CaV1.3 L‑Type Calcium Channels
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