Docking and PLS studies on a set of thiophenes RNA polymerase inhibitors against Staphylococcus aureus

Luciana Scotti, Edeltrudes de Oliveira Lima, Marcelo Sobral da Silva

  • 1Health Sciences Center, Federal University of Paraiba, Campus I 58051-970, João Pessoa, PB, Brazil. luciana.scotti@gmail.com.

Insights

New thiophene derivatives show promise in combating antibiotic-resistant Staphylococcus aureus by inhibiting RNA polymerase. This research identifies key structural features for developing novel anti-bacterial agents against this dangerous pathogen.

Area of Science:

  • Medicinal Chemistry
  • Computational Chemistry
  • Microbiology

Background:

  • Staphylococcus aureus is a common commensal but a dangerous pathogen, especially in chronic liver disease patients.
  • Antibiotic resistance, particularly to rifampin, is a growing threat, necessitating new therapeutic strategies.
  • RNA polymerase is a validated target for inhibiting S. aureus growth.

Purpose of the Study:

  • To investigate thiophene derivatives as potential inhibitors of Staphylococcus aureus RNA polymerase.
  • To identify structural features crucial for the anti-bacterial activity of these compounds.
  • To develop a predictive model for the activity of novel thiophene derivatives.

Main Methods:

  • Literature review and selection of 56 thiophene derivatives with reported RNA polymerase inhibitory activity.
  • Computational methods including Partial Least Squares (PLS) analysis, molecular docking, and Molecular Interaction Fields (MIFs) calculation.
  • In-house synthesis and testing of two thiophene derivatives for comparison.

Main Results:

  • Docking studies revealed that active thiophenes exhibit stronger interactions with the RNA polymerase active site compared to rifampicin.
  • A PLS model with two latent variables achieved high statistical significance (qcv(2) = 0.68, r(2) = 0.85) and external predictive power (rext(2) = 0.67).
  • The developed PLS model successfully predicted the activity of newly synthesized thiophene compounds, enabling the extraction of key structural activity relationships.

Conclusions:

  • Thiophene derivatives are effective inhibitors of Staphylococcus aureus RNA polymerase.
  • Computational methodologies (PLS, docking) are valuable tools for predicting and optimizing anti-bacterial compound activity.
  • This study provides a foundation for designing novel thiophene-based drugs to combat resistant S. aureus infections.

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