Faculty Research Profile

화학과

박철민

교수Cheol-Min Park

박철민

Cheol-Min Park

Biography

학력

Post-doctoral Fellow, Department of Chemistry, Stanford University, USA (1998)
Ph.D. Department of Chemistry, Seoul National University, Korea (1995)
M.S. Department of Chemistry, Seoul National University, Korea (1992)
B.S. Department of Chemistry, Seoul National University, Korea (1989)

주요 경력

Professor, Department of Chemistry, UNIST, Korea (2022 - present)
Associate Professor, Department of Chemistry, UNIST, Korea (2013 - 2022)
Associate Professor, Division of Chemistry and Biological Chemistry, Nanyang Technological University, Singapore (2008 - 2012)
Research Investigator, Global Pharmaceutical R&D, Abbott Laboratories (Abbvie), USA (2000 -2008)
Research Chemist, Central R&D, DuPont, USA (1998 - 2000)

Research

유기합성 및 의약화학 연구실

Synthetic and Medicinal Chemistry

Organic molecules are found as key players in many fields from materials to medicine. Our research focuses on the development of new synthetic methods that facilitate the design and synthesis of bioactive compounds and chemical tools for pharmacological studies.

The access to compounds with unique and diverse structures enables us to explore their potential as novel therapeutic leads, chemical switches and probes. In this regard, organic synthesis forms the foundation of our approach. Heterocyclic compounds represent an important class of compounds that are found in numerous bioactive natural products, drugs, and molecular probes. We have been engaged in the field of heterocycle synthesis by developing new synthetic methods based on metal catalysis. Also, we are actively engaged in developing strategies and methods to generate novel structures and to evaluate their pharmacological intervention including cancer.

Another approach we are undertaking involves rational drug design where the discovery process begins with a hypothesis that the modulation of a target may have therapeutic value. To this end, extensive use of modern discovery tools such as parallel synthesis, computer-aided drug design, x-ray crystallography, and NMR allows us to rapidly identify potential lead compounds and further optimization.

Organic molecules are found as key players in many fields from materials to medicine. Our research focuses on the development of new synthetic methods that facilitate the design and synthesis of bioactive compounds and chemical tools for pharmacological studies.

The access to compounds with unique and diverse structures enables us to explore their potential as novel therapeutic leads, chemical switches and probes. In this regard, organic synthesis forms the foundation of our approach. Heterocyclic compounds represent an important class of compounds that are found in numerous bioactive natural products, drugs, and molecular probes. We have been engaged in the field of heterocycle synthesis by developing new synthetic methods based on metal catalysis. Also, we are actively engaged in developing strategies and methods to generate novel structures and to evaluate their pharmacological intervention including cancer.

Another approach we are undertaking involves rational drug design where the discovery process begins with a hypothesis that the modulation of a target may have therapeutic value. To this end, extensive use of modern discovery tools such as parallel synthesis, computer-aided drug design, x-ray crystallography, and NMR allows us to rapidly identify potential lead compounds and further optimization.

연구분야

Organic synthesis, Medicinal chemistry

Organic synthesis, Medicinal chemistry

연구주제

Organic synthesis
Catalysis
Medicinal chemistry

Organic synthesis
Catalysis
Medicinal chemistry

국가연구개발사업 기술 분류체계

국가과학기술표준분류

NC. 화학 > NC02. 유기화학 > NC0203. 유기합성방법론

Outputs

논문

Angew. Chem. Int. Ed., "Electrosynthesis of Dihydropyrano[4,3‐b ]indoles Based on a Double Oxidative [3+3] Cycloaddition" Choi, S; Park, J; Yu, E; Sim, J; Park, CM*, 202004

Nat. Commun., "Alkyne–Alkene [2 + 2] cycloaddition based on visible light photocatalysis" Ha, S; Lee, Y; Kwak, Y; Mishra, A; Yu, E; Ryou, B; Park, CM*, 202005

ChemComm, “α-Diazo Oxime Ethers for N-Heterocycle Synthesis” Choi, S; Ha, S; Park, CM*, 201705

특허

Selective modifying method of nucleotide, Park, CM; Lee, YH; Yu, ES, 202003
Synthesis method of indolopyran derivative and indolopyran derivative synthesized by the same, Park, CM; Choi, SB; Park, JH; Yu, ES; Sim, JW, 202003