| 2010-09 | The efficient one-step chlorination of methylsulfanyl group on pyrimidine ring system with sulfuryl chloride | 하정미 |
| 2010-10 | Synthesis of aminoquinazoline derivatives and their antiproliferative activities against melanoma cell line | 하정미 |
| 2011-03 | Structure based design and syntheses of amino-1H-pyrazole amide derivatives as selective Raf kinase inhibitors in melanoma cells | 하정미 |
| 2010-09 | An efficient and enantioselective total synthesis of naturally occurring L-783277 | 하정미 |
| 2011-04 | Synthesis and Antiproliferative Activity of Pyridinylcarbonylpyrimidines Against Melanoma Cell Line | 하정미 |
| 2011-03 | Enhanced Solubility and Bioavailability of Flurbiprofen by Cycloamylose | 하정미 |
| 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 |
