Machine Learning-driven QSAR and Docking Pipeline for Identification of Amyloid Beta-A4 Inhibitors in Alzheimer’s Disease

Background/Purpose Alzheimer’s disease (AD) is a long-term neurodegenerative condition that leads to the gradual deterioration of nerve cells. The goal of this study is to use computational drug discovery (CDD) techniques to discover lead compounds that target Amyloid-beta A4 (AβA4) as a potential target for AD. Materials and Methods Quantitative structure-activity relationship (QSAR) modeling is used in this study to compare different machine learning (ML) models aimed at predicting the potency negative logarithm of IC 50 (pIC 50 ) of candidate compounds, which are then validated by molecular docking based on their binding affinity. A non-redundant dataset consisting of 1,241 compounds for AβA4 was retrieved from the ChEMBL database. 880 substructure fingerprints were used to define these compounds, followed by building 42 ML models and comparison. The Kennard–Stone algorithm was employed to select a diverse set of 30 compounds from the set of active inhibitors for testing. The application programming interface (API), named NeuroIC 50 , was developed and deployed. Results The histogram-based gradient boosting regression (HGBR) tree has achieved the optimal performance compared to other regression models, as determined by its root mean square error (RMSE) of 0.73, R 2 value of 0.65, and time efficiency of 0.78. Random forest regression (RFR)-HGBR-derived Gini index revealed the importance of features, include SubFP23, SubFP405, and SubFP577 in the compounds. Conclusion The lead compound (CHEMBL5080033) with a pIC 50 of 8.67 M and a binding energy of −7.6 kcal/mol was identified. This ML-based QSAR modeling and docking approach is an effective strategy for accelerating drug discovery.