professor

professor

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Jung-Mi Hah

Professor Jung-Mi Hah at Hanyang University College of Pharmacy, is s leading lab of medicinal chemistry, specially focusing on research of structure based, fragment-based protein kinase inhibitors. Dr. Hah received a Ph.D. degree from Northwestern University, Department of chemistry, Evanston, IL under guidance of professor Richard B. Silverman, who developed a milestone drug for neuropathic pain, Lyrica. Her postdoctoral training was then, completed in the Albert Einstein College of Medicine of Yeshiva University under the guidance of Professor David Lawrence, now the chair of medicinal and chemistry department at University of North Carolina.
The research interests of Prof. Hah’s group are Medicinal Chemistry, which is a big part in new drug discovery. In other words, it is to design small molecules that could fit into the “Receptor”, which includes receptor proteins, enzymes and deoxyribonucleic acid(DNA) and to synthesize them with efficient time and cost. As we live in the post genome era, we are able to determine the proteins within our bodies that invoke many types of disease. Furthermore, we are able to reduce the abnormal phenomenon of the proteins with small compound of 500 molecular weight. Since all these works are based on massive amount of money and long time, it could be called a composite art. The “Biological target protein” she is currently interested in is the “Protein Kinase”, and there are approximately 518 protein kinase discovered. It is a name or a collective of enzymes that is responsible for signal transduction between cells or inside the cells by transferring phosphoryl group to other proteins. Although the similarity of these kinase’s structure makes it very difficult to develop a selective inhibitor, it is a research area that is attractive and worth challenging. The protein kinases her group working on can be categorized into two part; 1. Anticancer drug discovery : since most of “ Protein Kinase” are related to cell proliferation, the inhibitor can be developed into anticancer agents; 2. Therapeutics for neurodegenerative disease : there are kinases which are especially related to “Neuronal cell apoptosis”, so it could be further developed into the cures for neurodegenerative disease such as Alzheimer’s disease, Parkinsonian disease, etc.

She teaches organic chemistry and medicinal chemistry for undergraduate and graduate students in Hanyang University. Her professional activity includes publishing research articles, abstracts, book and book chapters; patenting; peer-reviewing journal articles and grant proposals to the funding bodies of Korea. She is also a member of Korea Chemical Society, Korea Pharmaceutical Society.>
She is the author of more than 40 SCI articles including Nature(Structural Biology), Journal of American Chemical Society, Journal of Medicinal Chemistry, Bioorganic and Medicinal Chemistry and 35 patents.

Education

  • 1997 ~ 2002 Ph. D. Medicinal/Bioorganic Chemistry, Northwestern University, Evanston, IL
  • 1994 ~ 1996 M. S. Medicinal Chemistry, Seoul National University, Seoul, Korea
  • 1990 ~ 1994 B. S. College of Pharmacy, Seoul National University, Seoul, Korea Graduated Summa Cum Laude

Career 

  • 2020 Director ,Hanyang University ,Institute of Pharmaceutical Science and Technology
  • 2018 Professor, Department of Pharmacy, College of Pharmacy ,Hanyang University
  • 2013 Associate Professor, Department of Pharmacy, College of Pharmacy ,Hanyang University
  • 2010 Assistant Professor, Department of Pharmacy, college of Pharmacy, Hanyang University
  • 2007 Senior Research Scientist, Bioactive Molecules Center, Life / Health Division, KIST
  • 2003 Postdoctoral researcher, Research Professor Prof. David S. Lawrence, Department of Biochemistry, The Albert Einstein College of Medicine of Yeshiva University

Research Interests:

  • Development of protein kinase inhibitors as anticancer agent and therapeutics for neurodegenerative
  • Diseases. : Molecular targets are bRaf, JNK, FGFR
    Structure-based Drug Design
    Fragment-based drug discovery (in-silico, and NMR-based)
    Development of protein kinase sensing system, study of cell signaling.
  • Development of protein kinase sensing system, study of cell signaling.
    Library-Based strategy for the acquisition of potent inhibitors of Src Tyrosine kinase
    : Synthesized Peptide Library in high through-put parallel protocol and screened.
  • Mechanistic study of nitric oxide synthase and development of selective nNOS inhibitor
    Product studies for the oxidation of N-Allyl-L-arginine analogues by neuronal nitric oxide synthese (nNOS)”
    Substrate studies of N-hydroxy-L-arginine analogues by inducible NOS
    Peptidomometic approach for Potent and Selective Inhibitors of nNOS
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