2008-07 | Light-Mediated Liberation of Enzymatic Activity: "Small Molecule" Caged Protein Equivalents | 하정미 |
2001-02 | Mechanism of Nitric Oxide Synthase. Evidence that Direct Hydrogen Atom Abstraction from the O−H Bond of NG-Hydroxyarginine Is Not Relevant to the Mechanism | 하정미 |
2017-01 | Nec-1 alleviates cognitive impairment with reduction of A and tau abnormalities in APP/PS1 mice | 하정미 |
2017-01 | Nec-1 alleviates cognitive impairment with reduction of Aβ and tau abnormalities in APP/PS1 mice | 하정미 |
2012-05 | New diarylureas and diarylamides possessing acet(benz)amidophenyl scaffold: Design, synthesis, and antiproliferative activity against melanoma cell line | 하정미 |
2023-01 | Novel 1,4,5,6-tetrahydrocyclopenta[d]imidazole-5-carboxamide-based JNK3 inhibitors: Design, synthesis, molecular docking, and therapeutic potential in neurodegenerative diseases | 하정미 |
2022-11-10 | Novel 1,4,5,6-tetrahydrocyclopenta[d]imidazole-5-carboxamide-based JNK3 inhibitors: Design, synthesis, molecular docking, and therapeutic potential in neurodegenerative diseases | 하정미 |
2017-05 | Novel scaffold evolution through combinatorial 3D-QSAR model studies of two types of JNK3 inhibitors | 하정미 |
2021-10 | A Perspective on the Development of c-Jun N-terminal Kinase Inhibitors as Therapeutics for Alzheimer's Disease: Investigating Structure through Docking Studies | 하정미 |
2009-08 | Pharmacophore based 3D-QSAR study of VEGFR-2 inhibitors | 하정미 |
2021-12 | Rational 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 mutants | 하정미 |
2001-06 | Reduced Amide Bond Peptidomimetics. (4S)-N-(4-Amino-5-[aminoalkyl]aminopentyl)-N'-nitroguanidines, Potent and Highly Selective Inhibitors of Neuronal Nitric Oxide Synthase | 하정미 |
2012-02 | Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers | 하정미 |
2004-01 | Structural basis for dipeptide amide isoform-selective inhibition of neuronal nitric oxide synthase | 하정미 |
2011-03 | Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells | 하정미 |
2011-08 | Structure tuning of pyrazolylpyrrole derivatives as ERK inhibitors utilizing dual tools | 하정미 |
2013-04 | Syntheses and biological evaluation of 1-heteroaryl-2-aryl-1H-benzimidazole derivatives as c-Jun N-terminal kinase inhibitors with neuroprotective effects | 하정미 |
2011-11 | Syntheses of phenylpyrazolodiazepin-7-ones as conformationally rigid analogs of aminopyrazole amide scaffold and their antiproliferative effects on cancer cells | 하정미 |
2011-04 | Synthesis and Antiproliferative Activity of Pyridinylcarbonylpyrimidines Against Melanoma Cell Line | 하정미 |
2013-02 | Synthesis 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 inhibitors | 하정미 |
2010-10 | Synthesis of aminoquinazoline derivatives and their antiproliferative activities against melanoma cell line | 하정미 |
2009-10 | Synthesis of pyrrolo[2,3-d]pyrimidine derivatives and their antiproliferative activity against melanoma cell line | 하정미 |
2015-11 | Synthesis of stereochemically diverse cyclic analogs of tubulysins | 하정미 |
2024-03-26 | Targeting the CSF-1/CSF-1R Axis: Exploring the Potential of CSF1R Inhibitors in Neurodegenerative Diseases | 하정미 |
2010-09 | The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride | 하정미 |