QSAR-based Design of Schiff Base Inhibitors for Drug-resistant Salmonella typhi

Augustine Onuche Sule *

Department of Chemistry, Federal University Lokoja, Kogi, Nigeria.

Paul Bako Yacim

Department of Chemistry, Federal University Lokoja, Kogi, Nigeria.

Augustine Ohiole

Department of Chemistry, Federal University Lokoja, Kogi, Nigeria.

Fatogun Oluwayomi Patrick

Department of Chemistry, Federal University Lokoja, Kogi, Nigeria.

*Author to whom correspondence should be addressed.


Abstract

Salmonella typhi, a Gram-negative pathogen linked to typhoid disease, has shown concerning patterns of antibiotic resistance, highlighting the need for novel inhibitors. By using predicted Quantitative Structure-Activity Relationship (QSAR) models, this study aimed to identify the structural factors present in Schiff bases that have anti-Salmonella typhi activity. After a thorough collection of 43 Schiff bases was compiled, the minimum inhibitory concentrations (MIC) of each were transformed into pMIC values for analytical use. Molecular descriptors were obtained, and QSAR models were constructed using Genetic Function Approximation (GFA). Model 1 emerged as the most robust iteration, with validation metrics (R2 = 0.800, R2adj = 0.749, Q2 = 0.520, R2 - Q2 = 0.280, and R2pred = 0.642) reflecting substantial predictive capability. Model 1 identified Weta3.unity, a molecular weight descriptor, as the dominant descriptor that influences the anti-Salmonella typhi activity of Schiff bases. The findings highlight how molecular weight affects the efficacy of anti-Salmonella typhi, laying the groundwork for the logical development of more potent Schiff base derivatives.

Keywords: Salmonella typhi, QSAR, GFA, descriptors, inhibitors


How to Cite

Sule, Augustine Onuche, Paul Bako Yacim, Augustine Ohiole, and Fatogun Oluwayomi Patrick. 2025. “QSAR-Based Design of Schiff Base Inhibitors for Drug-Resistant Salmonella Typhi ”. Asian Journal of Chemical Sciences 15 (4):40-54. https://doi.org/10.9734/ajocs/2025/v15i4382.

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