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Molecular Docking and Antibacterial Activity of Campesterol Derivatives Against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa multiresistant strains.
Oliveira-Tintino, Cicera; Silva, Francisco; Santiago, Gilvandete; Pinto, Francisco; Pessoa, Otilia; Fonseca, Aluisio; Paulo, Cicera; Santos, Helcio; Marinho, Marcia; Santos, Jaqueline; Moura, Talyson; Freitas, Priscilla; Araújo, Ana Carolina; Almeida, Ray; Tintino, Saulo; Coutinho, Henrique.
Afiliação
  • Oliveira-Tintino C; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Silva F; Federal University of Ceara, chemistry, UFC, Fortaleza, BRAZIL.
  • Santiago G; Federal University of Ceara, chemistry, UFC, Fortaleza, BRAZIL.
  • Pinto F; Federal University of Ceara, chemistry, UFC, Fortaleza, BRAZIL.
  • Pessoa O; Federal University of Ceara, chemistry, UFC, CRATO, BRAZIL.
  • Fonseca A; University of International Integration of Afro-Brazilian Lusophony, chemistry, UNILAB, REDENÇÃO, BRAZIL.
  • Paulo C; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Santos H; Universidade Estadual Vale do Acarau, chemistry, UVA, SOBRAL, BRAZIL.
  • Marinho M; State University of Ceara, chemistry, UECE, Fortaleza, REUNION.
  • Santos J; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Moura T; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Freitas P; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Araújo AC; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Almeida R; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Tintino S; Regional University of Cariri, BIOLOGICAL CHEMISTRY, URCA, CRATO, BRAZIL.
  • Coutinho H; URCA, DQB, Av. Cel Antonio Luiz, 1161. Pimenta, Not Available, 63105-000, Crato, BRAZIL.
Chem Biodivers ; : e202401073, 2024 Sep 11.
Article em En | MEDLINE | ID: mdl-39258811
ABSTRACT
This work describes the evaluation the potentiating activity of antibiotics by campesterol (1) and its derivatives (2-11) against multiresistant strains of Staphylococcusaureus 10, Escherichia coli 06 and Pseudomonas aeruginosa 24 employing the microdilution test. When subjected to the in vitro potentiating activity bioassay, all compounds showed a potentiating effect associated with norfloxacin against E. coli and P. aeruginosa with a reduction in the MIC of the antibiotic of up to 75%. These compounds also reduced the MIC of gentamicin by 37% to 87% in S. aureus and E. coli. Additionally, molecular docking studies were conducted to gain a deeper understanding of the interactions between the appropriate proteins and the most effective compounds (2, 4, 9, and 10 against E. coli; 1, 2, 3, 5, 8, and 9 against S. aureus), including antibiotics. This paper registers for the first time the in vitro and in silico studies on the action of compounds 1-11 in antibiotic potentiation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Biodivers Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Biodivers Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça