Overview
Research in the Hong group focuses on using chemical tools, in particular small molecules, to understand the signaling pathways in biology. We synthesize biologically interesting natural products and screen small molecule libraries to identify modulators of biological processes. Then, we explore their modes of action in order to investigate intracellular signaling pathways and identify novel targets for drug design. In addition, we design and develop unique and efficient synthetic strategies that will allow rapid access to molecular complexity and structural diversity. Through multidisciplinary approaches, including organic synthesis, molecular biology, and cell biology, the cellular components and molecular events that embody cancer, immune response, and GPCR signaling have systematically been explored. Compounds employed in these studies could also advance the development of novel therapeutics for the treatment of human diseases.
Through multidisciplinary approaches, the cellular components and molecular events that embody cancer, immune response, and neurodegenerative diseases are systematically explored. Compounds employed in these studies could also advance the development of novel therapeutics for the treatment of human diseases.
- Synthesis of Natural Products and Study of Mode of Action: We synthesize biologically interesting natural products and explore the modes of action in order to investigate intracellular signaling pathways and identify novel targets for drug design. Completed target molecules include largazole (a marine natural product with HDAC inhibitory activity), brasilibactin A (a cytotoxic siderophore), manassantins A and B (natural products with anti-HIF-1 activity), and subglutinols A and B (natural products with immunosuppressive activity).
- Development of Novel Synthetic Methodology: We design and develop unique and efficient synthetic strategies which will allow rapid access to molecular complexity and structural diversity. A specific area of interest includes the development of novel methods for the stereoselective synthesis of substituted tetrahydrofurans and tetrahydropyrans.
- Screen of Small Molecule Libraries for Identification of Small Molecule Modulators of Biological Processes: With the advent of combinatorial chemistry and other synthetic technologies, it is feasible to prepare large collections of synthetic organic molecules. These libraries are useful in providing molecules that can be used to probe relevant biological pathways. We are interested in identification of modulators of biological processes, including drug abuse and neurodegenerative diseases.
Through multidisciplinary approaches, the cellular components and molecular events that embody cancer, immune response, and neurodegenerative diseases are systematically explored. Compounds employed in these studies could also advance the development of novel therapeutics for the treatment of human diseases.
Current Duke Appointments & Affiliations
Professor of Chemistry
·
2017 - Present
Chemistry,
Trinity College of Arts & Sciences
Associate Professor of Pharmacology and Cancer Biology
·
2013 - Present
Pharmacology & Cancer Biology,
Basic Science Departments
Member of the Duke Cancer Institute
·
2005 - Present
Duke Cancer Institute,
Institutes and Centers
Recent Scholarly Works
Stability-Based Proteomic Methods Add Value to Activity-Based Protein Profiling Studies.
Journal article ACS Chem Biol · June 11, 2026 Covalent inhibitors offer powerful therapeutic advantages over noncovalent inhibitors, but like noncovalent inhibitors, they require comprehensive profiling to define their on- and off-target activities. Here, we report on the use of two stability-based pr ... Full text Link to item CiteMESH1-mediated coenzyme A degradation drives ferroptosis sensitivity and muscle pathology.
Journal article J Clin Invest · June 1, 2026 CoA facilitates fatty acid synthesis, energy production, gene regulation, and antioxidant function. While CoA biosynthesis is well characterized, the mechanisms governing CoA degradation remain poorly understood. Here, we identify the Metazoan Homolog of S ... Full text Open Access Link to item CiteIdentification of 4,5,6,7-Tetrabromo-1H-benzotriazole (TBB) as a Small Molecule MESH1 Inhibitor that Suppresses Ferroptosis.
Journal article bioRxiv · February 20, 2026 Ferroptosis is a regulated form of cell death driven by iron-dependent lipid peroxidation and contributes to diverse pathologies including ischemia-reperfusion injury and neurodegenerative disorders. Current ferroptosis inhibitors largely function as nonsp ... Full text Link to item CiteRecent Grants
Pharmacological Sciences Training Program
Inst. Training Prgm or CMEPreceptor · Awarded by National Institutes of Health · 2025 - 2030LpxH Inhibitors as Novel Therapeutics Against Multidrug-resistant Enterobacterales
ResearchCo-Principal Investigator · Awarded by National Institutes of Health · 2025 - 2030TRPM8 in eye health and disease
ResearchCo-Principal Investigator · Awarded by National Institutes of Health · 2020 - 2029View All Grants
Education
The Scripps Research Institute ·
2001
Ph.D.
Seoul National University (South Korea) ·
1995
M.S.
Seoul National University (South Korea) ·
1993
B.S.