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Wan Nam

Yonsei University · 生化学・遺伝学・分子生物学

研究室紹介

Professor Wan Nam's research lab specializes in translational drug discovery, focusing on identifying novel small-molecule therapeutics for metabolic and neurological disorders. The lab leverages innovative technologies such as DNA-encoded library (DEL) screening and cell-based assays to discover high-affinity ligands and functional agonists targeting key receptors like GLP-1R. Current research directions include the development of orally available small-molecule drugs for type 2 diabetes and obesity, as well as identifying novel inhibitors for vestibular schwannoma (VS) with reduced toxicity. The lab integrates structural biology, functional pharmacology, and high-throughput screening to accelerate the discovery of targeted therapies.

drug discoveryGLP-1 receptorDNA-encoded librariessmall-molecule agonistsvestibular schwannoma

Research Overview

Papers
2
Total Citations
0
Papers (5y)
2
Primary Field
生化学・遺伝学・分子生物学

Research Output Trend

Figures are computed from collected data and may differ slightly.

Publications per year (5y)
2total
2016
2026
Citations per year (5y)
0total
20162026

Selected Papers

2
1
Article|0 citations·2026
Discovery of a new GLP-1 receptor agonist using DNA encoded-libraries and similarity search
Ju Ho Lee, Doyoun Kim, Hyejin Jeon, Sung Bum Park, Byumseok Koh, Byungho Lim, Kyeong A. Lee, Kyoung Jin Choi, Seong Soon Kim, Yujin Kwon, Jung-Hee Lim, Jung Hyun Jo
SJR Q2Results in ChemistryOA

The glucagon-like peptide-1 receptor (GLP-1R) is a validated therapeutic target for type 2 diabetes and obesity, yet discovery of orally available small-molecule agonists remains challenging. Here, we applied DNA-encoded library (DEL) technology to identify novel small-molecule binders and functional agonists of GLP-1R. Screening of DEL against recombinant GLP-1R revealed recurring structural motifs, particularly a chromane-containing building block. Selected high-scoring off-DNA compounds were

Molecular BiologyBiochemistry, Genetics and Molecular Biology
2
Article|0 citations·2016
약물스크리닝을 통해 청신경종양 세포를 억제하는 유효물질의 발굴
이세아, 이종대, 이호균, 남궁완

Objectives : Our knowledge of the molecular biology of vestibular schwannomas (VS) and the development of novel medical therapies for their treatment are increasing. Although several anticancer drugs have been tested in VS, new medical therapies without toxicity are needed. Therefore, we investigated to identify novel hit compounds for potential inhibitors of VS growth using a cell-based screening assay. Method : HEI-193 cells and Nf2 knockout SC4 cells were used to investigate the inhibitory ef

Research Areas

Molecular Biology

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