| 2011-08 | Structure tuning of pyrazolylpyrrole derivatives as ERK inhibitors utilizing dual tools | 하정미 |
| 2011-09 | A Python-based Docking Program Utilizing a Receptor Bound Ligand Shape: PythDock | 하정미 |
| 2011-11 | Syntheses of phenylpyrazolodiazepin-7-ones as conformationally rigid analogs of aminopyrazole amide scaffold and their antiproliferative effects on cancer cells | 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 |
| 2012-05 | New diarylureas and diarylamides possessing acet(benz)amidophenyl scaffold: Design, synthesis, and antiproliferative activity against melanoma cell line | 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 |
| 2012-05 | In silico binding free energy predictability with pi-pi interaction energy-augmented scoring function: Benzimidazole Raf inhibitors as a case study | 하정미 |
| 2014-08 | Design, synthesis and biological evaluation of benzyl 2-(1H-imidazole-1-yl) pyrimidine analogues as selective and potent Raf inhibitors | 하정미 |
| 2013-03 | 3D-QSAR studies of 1,2-diaryl-1H-benzimidazole derivatives as JNK3 inhibitors with protective effects in neuronal cells | 하정미 |
| 2015-06 | De Novo Design and Synthesis of a -Turn Peptidomimetic Scaffold and Its Application as JNK3 Allosteric Ligand | 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 |
| 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 |
| 2022-10 | Design and Synthesis of Aminopyrimidinyl Pyrazole Analogs as PLK1 Inhibitors Using Hybrid 3D-QSAR and Molecular Docking | 하정미 |
| 2017-01 | Nec-1 alleviates cognitive impairment with reduction of A and tau abnormalities in APP/PS1 mice | 하정미 |
| 2022-10 | Design of Novel IRAK4 Inhibitors Using Molecular Docking, Dynamics Simulation and 3D-QSAR Studies | 하정미 |
| 2023-01 | Discovery of novel imidazole chemotypes as isoform-selective JNK3 inhibitors for the treatment of Alzheimer's disease | 하정미 |
| 2014-09 | Click approach to the discovery of 1,2,3-triazolylsalicylamides as potent Aurora kinase inhibitors | 하정미 |
| 2023-05 | Carbamate JNK3 Inhibitors Show Promise as Effective Treatments for Alzheimer?s Disease: In Vivo Studies on Mouse Models | 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 |
| 2015-04 | Suppression of skin inflammation in keratinocytes and acute/chronic disease models by caffeic acid phenethyl ester | 배옥남 |
