Deep learning identifies TP-41 for methylglyoxal scavenging in Alzheimer's treatment
- Authors
- Park, Aron; Hong, Seong-Min; Lee, Yeeun; Lee, Jungeun; Jeon, Seunggyu; Seo, Seung-Yong; Lee, Jinhyuk; Kim, Seon-Hyeok; Ko, Eun Ji; Lee, Hae Ran; Jung, Sang Heon; Bae, Munhyung; Kang, Min Cheol; Park, Myoung Gyu; Nam, Seungyoon; Kim, Sun Yeou
- Issue Date
- Jan-2026
- Publisher
- Ivyspring International Publisher
- Keywords
- methylglyoxal; Alzheimer's disease; deep learning; memory impairment; drug discovery
- Citation
- Theranostics, v.16, no.3, pp 1103 - 1122
- Pages
- 20
- Indexed
- SCIE
- Journal Title
- Theranostics
- Volume
- 16
- Number
- 3
- Start Page
- 1103
- End Page
- 1122
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/82201
- DOI
- 10.7150/thno.111550
- ISSN
- 1838-7640
- Abstract
- Rationale: Increased levels of advanced glycation end products (AGEs) have been observed in the brain tissues of patients with Alzheimer's disease (AD). Methylglyoxal (MGO) is a potent precursor of AGEs. To date, there have been no reports of utilizing deep learning (DL) technologies to target MGO scavengers for the development of AD therapeutics. Therefore, DL-driven approaches may play a crucial role in identifying potential MGO scavengers and candidates for Alzheimer's treatment. Methods: We developed "DeepMGO," a novel DL-based MGO scavenging activity prediction model, trained on 2,262 MGO scavenging activity assays from 660 compounds. Using this approach, we identified and validated TP-41 as a potential MGO scavenger in a mouse model of memory impairment. Results: DeepMGO demonstrated robust predictive performance and identified novel compounds with high MGO scavenging activity. TP-41 ameliorated depression symptoms and memory deficits in mouse models. Conclusions: Using DeepMGO, we identified TP-41 as a potential therapeutic agent for AD.
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