Browsing "COLLEGE OF PHARMACY[E](약학대학)" byAuthor하정미

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Showing results 27 to 53 of 53

Issue DateTitleAuthor(s)
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
2012-02Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers하정미
2004-01Structural basis for dipeptide amide isoform-selective inhibition of neuronal nitric oxide synthase하정미
2011-03Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells하정미
2011-08Structure tuning of pyrazolylpyrrole derivatives as ERK inhibitors utilizing dual tools하정미
2013-04Syntheses and biological evaluation of 1-heteroaryl-2-aryl-1H-benzimidazole derivatives as c-Jun N-terminal kinase inhibitors with neuroprotective effects하정미
2011-11Syntheses of phenylpyrazolodiazepin-7-ones as conformationally rigid analogs of aminopyrazole amide scaffold and their antiproliferative effects on cancer cells하정미
2011-04Synthesis and Antiproliferative Activity of Pyridinylcarbonylpyrimidines Against Melanoma Cell Line하정미
2013-02Synthesis and biological evaluation of 1-(6-methylpyridin-2-yl)-5-(quinoxalin-6-yl)-1,2,3-triazoles as transforming growth factor-beta type 1 receptor ldnase inhibitors하정미
2010-10Synthesis of aminoquinazoline derivatives and their antiproliferative activities against melanoma cell line하정미
2009-10Synthesis of pyrrolo[2,3-d]pyrimidine derivatives and their antiproliferative activity against melanoma cell line하정미
2015-11Synthesis of stereochemically diverse cyclic analogs of tubulysins하정미
2010-09The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride하정미

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