Jiyong Hong
Affiliations: | Chemistry | Duke University, Durham, NC |
Area:
Synthesis of natural products, signaling pathways in biologyWebsite:
http://fds.duke.edu/db/aas/Chemistry/faculty/jiyong.hongGoogle:
"Jiyong Hong"Bio:
http://www.chem.duke.edu/~jiyong/labgroup/Hong_Lab/Group_Member.html
http://www.chem.duke.edu/~jiyong/labgroup/cv.pdf
Mean distance: 7.44 | S | N | B | C | P |
Parents
Sign in to add mentorDale L. Boger | grad student | 2001 | Scripps Institute | |
(Application of inverse electron demand Diels-Alder reactions in total synthesis of nothapodytine B, (-)-mappicine, Phomazazarin, and ent-(-)-roseophilin) | ||||
Peter G. Schultz | post-doc | 2001-2005 | Scripps Institute |
Children
Sign in to add traineeBumki Kim | grad student | Duke | |
Do Yeon Kwon | grad student | Duke | |
Megan Lainer | grad student | Duke | |
Minhee Lee | grad student | Duke | |
Hyunji Lee | grad student | Duke | |
Hyeri Park | grad student | Duke | |
Tesia Stephenson | grad student | Duke | |
Amanda C. Kasper | grad student | 2010 | Duke |
Yongcheng Ying | grad student | 2010 | Duke |
Joseph B. Baker | grad student | 2011 | Duke |
Kiyoun Lee | grad student | 2012 | Duke |
Heekwang Park | grad student | 2012 | Duke |
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Publications
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Byun JK, Lee SH, Moon EJ, et al. (2023) Manassantin A inhibits tumour growth under hypoxia through the activation of chaperone-mediated autophagy by modulating Hsp90 activity. British Journal of Cancer |
Hoy MJ, Park E, Lee H, et al. (2022) Structure-Guided Synthesis of FK506 and FK520 Analogs with Increased Selectivity Exhibit Therapeutic Efficacy against Cryptococcus. Mbio. e0104922 |
Webster CG, Park H, Ennis AF, et al. (2021) Synthetic efforts toward the bicyclo[3.2.1]octane fragment of rhodojaponin III. Tetrahedron Letters. 71 |
Kwak SH, Stephenson TN, Lee HE, et al. (2020) Evaluation of Manassantin A Tetrahydrofuran Core Region Analogues and Cooperative Therapeutic Effects with EGFR Inhibition. Journal of Medicinal Chemistry |
Cho J, Lee M, Cochrane CS, et al. (2020) Structural basis of the UDP-diacylglucosamine pyrophosphohydrolase LpxH inhibition by sulfonyl piperazine antibiotics. Proceedings of the National Academy of Sciences of the United States of America |
Park H, Christian L, Kim MJ, et al. (2019) Synthesis and Biological Evaluation of Subglutinol Analogs for Immunomodulatory Agents. Journal of Medicinal Chemistry |
Mashalidis EH, Kaeser B, Terasawa Y, et al. (2019) Chemical logic of MraY inhibition by antibacterial nucleoside natural products. Nature Communications. 10: 2917 |
Wojtaszek JL, Chatterjee N, Najeeb J, et al. (2019) A Small Molecule Targeting Mutagenic Translesion Synthesis Improves Chemotherapy. Cell |
Hong J, Lee H, Sylvester K, et al. (2019) Synthesis and Analysis of Natural Product-Like Macrocycles via Tandem Oxidation/Oxa-Conjugate Addition Reactions. Chemistry (Weinheim An Der Bergstrasse, Germany) |
Lee M, Zhao J, Kwak SH, et al. (2019) Structure-Activity Relationship of Sulfonyl Piperazine LpxH Inhibitors Analyzed by an LpxE-Coupled Malachite Green Assay. Acs Infectious Diseases |