Computational in silico methods offer a powerful alternative to animal-based toxicity testing, which remains time-consuming, expensive, and ethically challenging. In practice, QSAR and read-across (RA) are among the most widely explored approaches, yet both suffer from important limitations, including end point-specific modeling, restricted applicability domains, nonquantitative or subjective analogue selection, and sensitivity to biases in chemical space coverage. To address these limitations, this study introduces ToxCML, a large-scale hybrid multifeature consensus quantitative RA Structure-Activity Relationship (mfCoQ-RASAR) platform that unifies consensus QSAR and similarity-based consensus RA into a weight-optimized workflow for predicting 18 toxicity end points across 54,601 unique chemicals. The framework combines multiple molecular representations (MACCS, Morgan, atom pair fingerprints, RDKit fingerprints, and physicochemical descriptors) with machine-learning-based QSAR and k-NN RA models and incorporates tiered applicability-domain analysis and chemical-space mapping that indicate broadly overlapping training-test distributions and in-domain coverage generally exceeding 95% across end points. Across all end points and evaluation settings involving unseen test sets or external validation sets, the hybrid mfCoQ-RASAR models achieve strong discrimination and accuracy (AUC approximately 0.86-0.99; BACC 0.73-0.98), with a consistent performance hierarchy in which mfCoQ-RASAR provides the highest or near-highest performance, consensus QSAR remains highly competitive, and consensus RA, while weaker, still offers informative predictive and analogue-based discriminatory capability. These results indicate that our framework delivers reliable, chemically well-contextualized, and broadly applicable multiend point toxicity predictions for unseen compounds and may support large-scale toxicity screening, hazard prioritization, and efforts to reduce animal testing in regulatory and industrial settings. The ToxCML platform is accessible through a public web server available at http://cardiosim.metaheart.kr:8080/.
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Fauzan Syarif Nursyafi
Kumoh National Institute of Technology
Muhammad Adnan Pramudito
Kumoh National Institute of Technology
Yunendah Nur Fuadah
Telkom University
Journal of Chemical Information and Modeling
Computational Physics (United States)
Kumoh National Institute of Technology
Heart Foundation
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Nursyafi et al. (Mon,) studied this question.
synapsesocial.com/papers/69e07c632f7e8953b7cbda25 — DOI: https://doi.org/10.1021/acs.jcim.6c00357
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