Improving the SSIR Method: Implementation of an Exhaustive Multilevel Scan for Categorical Variables

The Superposing Significant Interaction Rules (SSIR) method is briefly revisited. The original version of the algorithm consists of dealing with rules that evaluate the individual presence or absence of substituents in the molecular structures of a combinatorial chemical family. Here, an extension is developed, allowing for the systematic consideration of multilevel conditions, i.e., the presence or absence of not only single residues but also groups of residues attached to a particular substitution site. This possibility expands the universe of possible definable rules. Then, the original SSIR version becomes a particular case of the framework presented in this manuscript. A numerical example involving a family of anti-HIV compounds is provided to illustrate the application and potential of the extended method. Procedures for generating predictions for new in silico virtual molecular structures are also shown.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-02-19
DOI
https://doi.org/10.3390/ijms27041972
Primary Topic
Computational Drug Discovery Methods
Type
article
Field-Weighted Citation Impact
0.00

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article

Improving the SSIR Method: Implementation of an Exhaustive Multilevel Scan for Categorical Variables

Emili Besalú
International Journal of Molecular Sciences
Computational Drug Discovery Methods
article

Improving the SSIR Method: Implementation of an Exhaustive Multilevel Scan for Categorical Variables

Emili Besalú
article en

Abstract

The Superposing Significant Interaction Rules (SSIR) method is briefly revisited. The original version of the algorithm consists of dealing with rules that evaluate the individual presence or absence of substituents in the molecular structures of a combinatorial chemical family. Here, an extension is developed, allowing for the systematic consideration of multilevel conditions, i.e., the presence or absence of not only single residues but also groups of residues attached to a particular substitution site. This possibility expands the universe of possible definable rules. Then, the original SSIR version becomes a particular case of the framework presented in this manuscript. A numerical example involving a family of anti-HIV compounds is provided to illustrate the application and potential of the extended method. Procedures for generating predictions for new in silico virtual molecular structures are also shown.

International Journal of Molecular SciencesVol. 27(4)
Universitat de Girona (ES)
Universitat de Girona, Generalitat de Catalunya
Good health and well-being
Openalex Percentile: Top 48%
Computational Drug Discovery Methods
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