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Showing results 13 to 42 of 54

Issue DateTitleAuthor(s)
2015-06De Novo Design and Synthesis of a -Turn Peptidomimetic Scaffold and Its Application as JNK3 Allosteric Ligand하정미
2021-04Design and Synthesis of a Novel PLK1 Inhibitor Scaffold Using a Hybridized 3D-QSAR Model하정미
2022-10Design and Synthesis of Aminopyrimidinyl Pyrazole Analogs as PLK1 Inhibitors Using Hybrid 3D-QSAR and Molecular Docking하정미
2022-10Design of Novel IRAK4 Inhibitors Using Molecular Docking, Dynamics Simulation and 3D-QSAR Studies하정미
2014-08Design, synthesis and biological evaluation of benzyl 2-(1H-imidazole-1-yl) pyrimidine analogues as selective and potent Raf inhibitors하정미
2019-02Design, synthesis, and in vitro evaluation of N-(3-(3-alkyl-1H-pyrazol-5-yl) phenyl)-aryl amide for selective RAF inhibition하정미
2000-06Deuterium isotope effects and product studies for the oxidation of Nω-allyl-l-arginine and Nω-allyl-Nω-hydroxy-l-arginine by neuronal nitric oxide synthase하정미
2020-03Discovery of 1-Pyrimidinyl-2-Aryl-4,6-Dihydropyrrolo [3,4-d]Imidazole-5(1H)-Carboxamide as a Novel JNK Inhibitor하정미
2019-12Discovery of 3-alkyl-5-aryl-1-pyrimidyl-1H-pyrazole derivatives as a novel selective inhibitor scaffold of JNK3하정미
2015-09Discovery of 4-arylamido 3-methyl isoxazole derivatives as novel FMS kinase inhibitors하정미
2020-04Discovery of 5-methyl-N-(2-arylquinazolin-7-yl)isoxazole-4-carboxamide analogues as highly selective FLT3 inhibitors하정미
2021-10Discovery of a Potent and Selective JNK3 Inhibitor with Neuroprotective Effect Against Amyloid beta-Induced Neurotoxicity in Primary Rat Neurons하정미
2016-02Discovery of highly selective CRAF inhibitors, 3-carboxamido-2H-indazole-6-arylamide: In silico FBLD design, synthesis and evaluation하정미
2018-05Discovery of novel 4-aryl-thieno[1,4] diazepin-2-one derivatives targeting multiple protein kinases as anticancer agents하정미
2023-01Discovery of novel imidazole chemotypes as isoform-selective JNK3 inhibitors for the treatment of Alzheimer's disease하정미
2011-03Enhanced Solubility and Bioavailability of Flurbiprofen by Cycloamylose하정미
2021-11Generation of Non-Nucleotide CD73 Inhibitors Using a Molecular Docking and 3D-QSAR Approach하정미
2009-11Hologram and Receptor-Guided 3D QSAR Analysis of Anilinobipyridine JNK3 Inhibitors하정미
2012-05In silico binding free energy predictability with pi-pi interaction energy-augmented scoring function: Benzimidazole Raf inhibitors as a case study하정미
2008-07Light-Mediated Liberation of Enzymatic Activity: "Small Molecule" Caged Protein Equivalents하정미
2001-02Mechanism of Nitric Oxide Synthase. Evidence that Direct Hydrogen Atom Abstraction from the O−H Bond of NG-Hydroxyarginine Is Not Relevant to the Mechanism하정미
2017-01Nec-1 alleviates cognitive impairment with reduction of A and tau abnormalities in APP/PS1 mice하정미
2017-01Nec-1 alleviates cognitive impairment with reduction of Aβ and tau abnormalities in APP/PS1 mice하정미
2012-05New diarylureas and diarylamides possessing acet(benz)amidophenyl scaffold: Design, synthesis, and antiproliferative activity against melanoma cell line하정미
2023-01Novel 1,4,5,6-tetrahydrocyclopenta[d]imidazole-5-carboxamide-based JNK3 inhibitors: Design, synthesis, molecular docking, and therapeutic potential in neurodegenerative diseases하정미
2017-05Novel scaffold evolution through combinatorial 3D-QSAR model studies of two types of JNK3 inhibitors하정미
2021-10A Perspective on the Development of c-Jun N-terminal Kinase Inhibitors as Therapeutics for Alzheimer's Disease: Investigating Structure through Docking Studies하정미
2009-08Pharmacophore based 3D-QSAR study of VEGFR-2 inhibitors하정미
2021-12Rational design and synthesis of 2-(1H-indazol-6-yl)-1H-benzo[d]imidazole derivatives as inhibitors targeting FMS-like tyrosine kinase 3 (FLT3) and its mutants하정미
2001-06Reduced Amide Bond Peptidomimetics. (4S)-N-(4-Amino-5-[aminoalkyl]aminopentyl)-N'-nitroguanidines, Potent and Highly Selective Inhibitors of Neuronal Nitric Oxide Synthase하정미

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