Aug 2026· International Conference on Circuit, Power and Computing Technologies· pp. 1954-1960· 0 citations· 25 references
Abstract
Drug classification plays a critical role in medicine as it aids in selecting the best medicines for an individual’s needs based on their individual characteristics and history. Computational methods are increasingly used in drug discovery to build structure-activity models for large chemical databases. This study introduces a scalable ML approach for drug classification based on scaffolds using SMILES from the ChEMBL database. The approach uses RDKit for physicochemical descriptor extraction, Bemis-Murcko scaffolds for target construction and employs feature selection, encoding, RobustScaler normalization and SMOTE for balancing classes. Models include Random Forest, XGBoost, and a Stacking Ensemble, with accuracy, precision, recall, F1-score, and ROC-AUC as evaluation metrics. The experimental findings show that the Stacking Ensemble outperforms Random Forest (88.06%) and XGBoost (85.91%), achieving an accuracy of 89.15% and a ROC-AUC of 98.29%, suggesting better generalization. The results demonstrate that ensemble and tree-based learning methods outperform traditional models and LSTM in scaffold classification. The novel approach provides a rapid, scalable, and precise framework that increases the efficiency of virtual screening and offers a reliable approach to AI-based decision-making in drug discovery.
PredictRx shows how AI-driven predictive modeling which can speed up molecular screening and early-stage breast cancer medication discovery shows how AI-driven predictive modeling can speed up molecular screening and early-stage breast cancer medication discovery.
Ritu Chauhan, Neha Pandey, M. Zuhairi· Frontiers in Artificial Inte...· 0 citations
This study combines a QSAR model and machine learning algorithms to predict antibacterial activities of potential novel drugs based on chemical information and revealed that descriptors relating to the electrotopology and β-lactam structures of compounds were the top contributors to model predictability.
Jiratchaya Nakbang, Chonthicha Arbsuwan, S. Prom-on et al.· PLOS Digital Health· 0 citations
This evidence-based literature review critically examines the evolution and application of computational technologies across the pharmaceutical pipeline, ranging from early expert systems like DENDRAL, computer-aided drug design (CADD), and quantitative structure-activity relationship (QSAR) modeling to AlphaFold 3 bio...
Leonardo Mairene Muniz· Brazilian Journal of Health...· 0 citations
The development of an ensemble machine learning pipeline for predicting resistance gene functions using the Comprehensive Antibiotic Resistance Database (CARD) demonstrates superior performance while maintaining computational efficiency, making it suitable for deployment in resourceconstrained environments.
Princewill Ahumaraeze, Ofonime Dominic Okon, P. Asuquo et al.· E3S Web of Conferences· 0 citations
This review systematically summarizes the latest research progress in druggable protein prediction algorithms, providing a comprehensive analysis across three dimensions: data resources, feature engineering, and predictive models.
Hong-Qi Zhang, Hong-Ling Wang, Shang-Hua Liu et al.· Current Drug Targets· 0 citations
This review systematically summarizes the latest developments in heterogeneous graph neural networks, protein language models, and generative artificial intelligence, pointing out the problems currently being addressed in research such as data sparsity and cold start as well as the manifestations of general machine lea...
Qi-Zhong Yang· ITM Web of Conferences· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.