Jee-Young Lee
Yonsei University
12 Papers
88 Citations
Jee-Young Lee is an academic researcher from Yonsei University. The author has contributed to research in topics: Melanophilin & Pharmacophore. The author has an hindex of 6, co-authored 12 publications.
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Papers
The natural phytochemical dehydroabietic acid is an anti-aging reagent that mediates the direct activation of SIRT1.
Juewon Kim,Juewon Kim,Young Gyu Kang,Jee-Young Lee,Dong hwa Choi,Cho Young Uk,Jae Min Shin,Jun Seong Park,John Hwan Lee,Wan Gi Kim,Dae Bang Seo,Tae Ryong Lee,Yusei Miyamoto,Kyoung Tai No +13 more
TL;DR: The results demonstrate that the anti-aging effects are the first identified biological property of DAA and that the direct activation of SIRT1 enzymatic activity suggests the potential use of this natural diterpene, or related compounds, in age-related diseases or as a preventive reagent against the aging process.
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Patent
Fumagillol derivatives and preparing method thereof
Cheol-Kyu Han,Jeonghyeok Yoon,Seung-Moak Kim,Nam-Doo Kim,Byung-Ha Chang,Jee-Young Lee,Taebo Sim +6 more
- 11 Jun 2002
TL;DR: In this article, a fumagillol compound was used as an angiogenesis inhibiting agent showing a superior angeogenesis inhibitory effect with less toxicity, but also as a cancer metastasis inhibitor and a therapeutic agent against cancer and other various inflammatory diseases such as rheumatic disease, psoriasis, etc.
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Hesperidin Suppresses Melanosome Transport by Blocking the Interaction of Rab27A-Melanophilin.
Bora Kim,Jee-Young Lee,Ha Yeon Lee,Ky Youb Nam,Jong Il Park,Su Min Lee,Jin Eun Kim,Joo Dong Lee,Jae Sung Hwang +8 more
TL;DR: It is suggested that hesperidin is a useful inhibitor of melanosome transport and it might be applied to whitening agent.
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Identification of Novel Rab27a/Melanophilin Blockers by Pharmacophore-Based Virtual Screening
Jong Young Joung,Ha Yeon Lee,Jong Il Park,Jee-Young Lee,Byung Ha Chang,Kyoung Tai No,Ky Youb Nam,Jae Sung Hwang +7 more
TL;DR: To identify novel compounds to inhibit binding interface between Rab27a and melanophilin, a pharmacophore model was built based on a modeled 3D structure of the protein complex that describes the essential binding residues in the intermolecular interaction and two hydroxyl functional groups were found to be critical for blocking the interMolecular binding.
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Comparative homology modeling and ligand docking study of human catechol-O-methyltransferase for antiparkinson drug design
Jee-Young Lee,Yangmee Kim +1 more
TL;DR: Analysis of ligand-protein binding model implies that Arg201 on hCOMT plays important roles in the interactions with COMT inhibitors, which may give insight to develop new ways of antiparkinson drug.
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