Predicting mutagenicity of aromatic and heteroaromatic amine mutagens using a newly developed set of Laplacian matrix-based graph invariants

This paper presents an effort for development of predictive quantitative structure-activity relationship (QSAR) models to assess mutagenicity of a set of 95 aromatic and heteroaromatic amines using newly developed set of Laplacian matrix-based molecular descriptors applying graph convolution. In order to calculate these descriptors, we used (1) properties of isolated atoms, (2) properties of the atoms, which arise from their inclusion in molecular structures, and (3) properties derived from the graphs that represent the molecules. The QSAR models developed are based on counter-propagation artificial neural network algorithm. The optimization was performed in an automated manner using genetic algorithm for (1) selection of the most suitable descriptors as well as for (2) selection of the most suitable parameters of the neural networks. Results presented in this study show that this new type of descriptors, reported in this paper, encode structural information capable of predicting TA98 Ames’ mutagenicity of the amines.

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Publication Details

Journal
Acta chimica slovenica
Published
2026-06-18
DOI
https://doi.org/10.17344/acsi.2026.9757
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

Predicting mutagenicity of aromatic and heteroaromatic amine mutagens using a newly developed set of Laplacian matrix-based graph invariants

Subhash C. Basak, Igor Kuzmanovski
Acta chimica slovenica
Computational Drug Discovery Methods
article

Predicting mutagenicity of aromatic and heteroaromatic amine mutagens using a newly developed set of Laplacian matrix-based graph invariants

Subhash C. Basak, Igor Kuzmanovski
article en

Abstract

This paper presents an effort for development of predictive quantitative structure-activity relationship (QSAR) models to assess mutagenicity of a set of 95 aromatic and heteroaromatic amines using newly developed set of Laplacian matrix-based molecular descriptors applying graph convolution. In order to calculate these descriptors, we used (1) properties of isolated atoms, (2) properties of the atoms, which arise from their inclusion in molecular structures, and (3) properties derived from the graphs that represent the molecules. The QSAR models developed are based on counter-propagation artificial neural network algorithm. The optimization was performed in an automated manner using genetic algorithm for (1) selection of the most suitable descriptors as well as for (2) selection of the most suitable parameters of the neural networks. Results presented in this study show that this new type of descriptors, reported in this paper, encode structural information capable of predicting TA98 Ames’ mutagenicity of the amines.

Acta chimica slovenicaVol. 73
Openalex Percentile: Top 5%
Computational Drug Discovery Methods
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Predicting mutagenicity of aromatic and heteroaromatic amine mutagens using a newly developed set of Laplacian matrix-based graph invariants — Subhash C. Basak, Igor Kuzmanovski · Acta chimica slovenica (2026) | TGRS Research Map | TGRS