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LY2183240 regioisomers act as competitive and selective inhibitors of class C ß-lactamases.
de Resende, Pedro Ernesto; Soares, Sarah; Zloh, Mire; Gibbons, Simon; Stapleton, Paul.
Afiliação
  • de Resende PE; UCL School of Pharmacy, Research Department of Pharmaceutical and Biological Chemistry, University College London, London, UK. Electronic address: pedroderesende@gmail.com.
  • Soares S; UCL School of Pharmacy, Research Department of Pharmaceutical and Biological Chemistry, University College London, London, UK.
  • Zloh M; UCL School of Pharmacy, Research Department of Pharmaceutical and Biological Chemistry, University College London, London, UK.
  • Gibbons S; UCL School of Pharmacy, Research Department of Pharmaceutical and Biological Chemistry, University College London, London, UK; Centre for Natural Products Discovery, Liverpool John Moores University, Liverpool, UK.
  • Stapleton P; UCL School of Pharmacy, Research Department of Pharmaceutical and Biological Chemistry, University College London, London, UK.
Int J Antimicrob Agents ; 61(5): 106774, 2023 May.
Article em En | MEDLINE | ID: mdl-36893812
ABSTRACT
The regioisomers of the anandamide-acting drug LY2183240 exhibited specific potent and competitive inhibitory activities against class C ß-lactamases. More explicitly, the 1,5- and 2,5-regioisomers inhibited AmpC from Enterobacter hormaechei (formerly Enterobacter cloacae) with inhibitor binding affinity values of 1.8 µM and 2.45 µM, respectively. Structural molecular modelling studies revealed the interaction of the regioisomers with the relevant residues of the catalytic site of cephalosporinase from E. hormaechei P99, which included Tyr150, Lys315 and Thr316.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Cefalosporinase Idioma: En Revista: Int J Antimicrob Agents Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Beta-Lactamases / Cefalosporinase Idioma: En Revista: Int J Antimicrob Agents Ano de publicação: 2023 Tipo de documento: Article