EXPLAINABLE ARTIFICIAL NEURAL NETWORKS FOR TABULAR DATA: IDENTIFYING STRUCTURAL, ELECTRONIC AND PHYSICOCHEMICAL DETERMINANTS OF PHARMACEUTICAL COMPOUND-INDUCED RESPIRATORY TOXICITY

Respiratory toxicity induced by pharmaceutical compounds is a major concern in drug discovery and development, emphasizing the need for reliable computational approaches to identify potentially hazardous compounds at an early stage. In this study, an artificial neural network (ANN) integrated with eXplainable Artificial Intelligence (XAI) was developed for the binary classification of pharmaceutical compounds as respiratory toxic or non-toxic using a tabular dataset of molecular descriptors. Model performance was evaluated through ten-fold cross-validation and external validation using accuracy, precision, recall, F1-score, Matthews correlation coefficient (MCC), and area under the receiver operating characteristic curve (AUC-ROC). During internal validation, the ANN achieved an accuracy of 84.05% and an AUC of 91.36%. On the external test set, the model yielded an accuracy of 83.40%, precision of 85.58%, recall of 85.19%, F1-score of 85.38%, MCC of 0.66, and AUC-ROC of 89.53%, demonstrating robust predictive performance and satisfactory generalization to unseen compounds. SHapley Additive exPlanations (SHAP) analysis was further employed to interpret the ANN predictions and identify the molecular characteristics most strongly associated with model output. The most influential descriptors included nBase, BCUTp-1h, SssO, minssCH2, JGI8, maxHBd, nHeteroRing, GATS2m, ETA_BetaP_ns_d, GATS1e. Collectively, these descriptors encode complementary information related to basicity, heterocyclic structure, local electronic environments, hydrogen-bonding characteristics, atomic polarizability, charge distribution, atomic mass, electronegativity, and molecular topology. The SHAP findings suggest that respiratory toxicity predictions are governed by the combined contribution of multiple structural and physicochemical characteristics rather than by a single molecular property.

Authors

Institutions

Publication Details

Journal
GSC Biological and Pharmaceutical Sciences
Published
2026-11-01
DOI
https://doi.org/10.30574/gscbps.2026.37.2.0372
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

EXPLAINABLE ARTIFICIAL NEURAL NETWORKS FOR TABULAR DATA: IDENTIFYING STRUCTURAL, ELECTRONIC AND PHYSICOCHEMICAL DETERMINANTS OF PHARMACEUTICAL COMPOUND-INDUCED RESPIRATORY TOXICITY

Kouakou Kouakou, Aubin N’guessan, Désiré MELEDJE, Donatien Zamblé
GSC Biological and Pharmaceutical Sciences
Computational Drug Discovery Methods
article

EXPLAINABLE ARTIFICIAL NEURAL NETWORKS FOR TABULAR DATA: IDENTIFYING STRUCTURAL, ELECTRONIC AND PHYSICOCHEMICAL DETERMINANTS OF PHARMACEUTICAL COMPOUND-INDUCED RESPIRATORY TOXICITY

Kouakou Kouakou, Aubin N’guessan, Désiré MELEDJE, Donatien Zamblé
article en

Abstract

Respiratory toxicity induced by pharmaceutical compounds is a major concern in drug discovery and development, emphasizing the need for reliable computational approaches to identify potentially hazardous compounds at an early stage. In this study, an artificial neural network (ANN) integrated with eXplainable Artificial Intelligence (XAI) was developed for the binary classification of pharmaceutical compounds as respiratory toxic or non-toxic using a tabular dataset of molecular descriptors. Model performance was evaluated through ten-fold cross-validation and external validation using accuracy, precision, recall, F1-score, Matthews correlation coefficient (MCC), and area under the receiver operating characteristic curve (AUC-ROC). During internal validation, the ANN achieved an accuracy of 84.05% and an AUC of 91.36%. On the external test set, the model yielded an accuracy of 83.40%, precision of 85.58%, recall of 85.19%, F1-score of 85.38%, MCC of 0.66, and AUC-ROC of 89.53%, demonstrating robust predictive performance and satisfactory generalization to unseen compounds. SHapley Additive exPlanations (SHAP) analysis was further employed to interpret the ANN predictions and identify the molecular characteristics most strongly associated with model output. The most influential descriptors included nBase, BCUTp-1h, SssO, minssCH2, JGI8, maxHBd, nHeteroRing, GATS2m, ETA_BetaP_ns_d, GATS1e. Collectively, these descriptors encode complementary information related to basicity, heterocyclic structure, local electronic environments, hydrogen-bonding characteristics, atomic polarizability, charge distribution, atomic mass, electronegativity, and molecular topology. The SHAP findings suggest that respiratory toxicity predictions are governed by the combined contribution of multiple structural and physicochemical characteristics rather than by a single molecular property.

GSC Biological and Pharmaceutical SciencesVol. 37(2)
Université Nangui Abrogoua (CI)
Openalex Percentile: Top 14%
Computational Drug Discovery Methods
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon