AI-Driven discovery of brain-penetrant mTOR-independent autophagy enhancers for Alzheimer’s disease

Current Alzheimer's disease therapies offer limited efficacy and are often accompanied by significant side effects, underscoring the urgent need for new treatment strategies. Enhancing autophagy represents a promising therapeutic approach, yet most known autophagy inducers act through the mTOR-dependent pathway, which broadly affects cellular metabolism and proliferation, and their clinical potential is further limited by poor blood-brain barrier (BBB) penetration. To address these twin challenges, an artificial intelligence (AI)-driven platform named DeepDrugDiscovery was developed, shifting the focus from traditional structure-based screening toward a mechanism-centric strategy for identifying mTOR-independent autophagy enhancers with brain penetrability. The platform screened over one million molecules and identified two lead compounds, Ombuin and 2-Hydroxycinnamic acid, which were experimentally shown to clear pathogenic tau and amyloid-β aggregates and restore memory function in both worm and mouse models of Alzheimer's disease. Notably, Ombuin exhibited robust brain exposure, confirming accurate BBB prediction. Released as an open-source resource, DeepDrugDiscovery demonstrates a scalable, AI-powered pipeline for discovering mechanism-based therapeutics.

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Publication Details

Journal
Autophagy
Published
2026-05-31
DOI
https://doi.org/10.1080/15548627.2026.2679639
Primary Topic
Autophagy in Disease and Therapy
Type
article
Field-Weighted Citation Impact
0.00

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article

AI-Driven discovery of brain-penetrant mTOR-independent autophagy enhancers for Alzheimer’s disease

Zhangming Niu, Xu‐Xu Zhuang, Wenfan Wu, Xianglu Xiao et al.
Autophagy
Autophagy in Disease and Therapy
article

AI-Driven discovery of brain-penetrant mTOR-independent autophagy enhancers for Alzheimer’s disease

Zhangming Niu, Xu‐Xu Zhuang, Wenfan Wu, Xianglu Xiao, Jia-Hong Lu, Evandro F. Fang, Guang Yang, Yu Dong
article en

Abstract

Current Alzheimer's disease therapies offer limited efficacy and are often accompanied by significant side effects, underscoring the urgent need for new treatment strategies. Enhancing autophagy represents a promising therapeutic approach, yet most known autophagy inducers act through the mTOR-dependent pathway, which broadly affects cellular metabolism and proliferation, and their clinical potential is further limited by poor blood-brain barrier (BBB) penetration. To address these twin challenges, an artificial intelligence (AI)-driven platform named DeepDrugDiscovery was developed, shifting the focus from traditional structure-based screening toward a mechanism-centric strategy for identifying mTOR-independent autophagy enhancers with brain penetrability. The platform screened over one million molecules and identified two lead compounds, Ombuin and 2-Hydroxycinnamic acid, which were experimentally shown to clear pathogenic tau and amyloid-β aggregates and restore memory function in both worm and mouse models of Alzheimer's disease. Notably, Ombuin exhibited robust brain exposure, confirming accurate BBB prediction. Released as an open-source resource, DeepDrugDiscovery demonstrates a scalable, AI-powered pipeline for discovering mechanism-based therapeutics.

Autophagy
King's College London (GB), University of Oslo (NO), University of Macau (MO), Akershus University Hospital (NO), Guangzhou Experimental Station (CN), Royal Brompton Hospital (GB), NORCE Research AS (NO), Minerals Technologies (United States) (US), Mindray (China) (CN), Imperial College London (GB), Huazhong University of Science and Technology (CN)
Royal Society, National Natural Science Foundation of China, NIHR Imperial Biomedical Research Centre
Openalex Percentile: Top 6%
Autophagy in Disease and Therapy
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