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Cellular Studies of an Aminoglycoside Potentiator Reveal a New Inhibitor of Aminoglycoside Resistance.
Guan, Jinming; Vong, Kenward; Wee, Kathleen; Fakhoury, Johans; Dullaghan, Edie; Auclair, Karine.
Afiliação
  • Guan J; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, H3A 0B8, Canada.
  • Vong K; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, H3A 0B8, Canada.
  • Wee K; Target Validation Division, The Centre for Drug Research and Development, 2405 Westbrook Mall, 4th Floor, Vancouver, British Columbia, V6T 1Z3, Canada.
  • Fakhoury J; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, H3A 0B8, Canada.
  • Dullaghan E; Target Validation Division, The Centre for Drug Research and Development, 2405 Westbrook Mall, 4th Floor, Vancouver, British Columbia, V6T 1Z3, Canada.
  • Auclair K; Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec, H3A 0B8, Canada.
Chembiochem ; 19(19): 2107-2113, 2018 10 04.
Article em En | MEDLINE | ID: mdl-30059603
Aminoglycosides are a group of broad-spectrum antibiotics that have been used in the clinic for almost a century. The rapid spread of bacterial genes coding for aminoglycoside-modifying enzymes has, however, dramatically decreased the utility of aminoglycosides. We have previously reported several aminoglycoside potentiators that work by inhibiting aminoglycoside N-6'-acetyltransferase, one of the most common determinants of aminoglycoside resistance. Among these, prodrugs that combine the structure of an aminoglycoside with that of pantothenate into one molecule are especially promising. We report here a series of cellular studies to investigate the activity and mechanism of action of these prodrugs further. Our results reveal a new aminoglycoside resistance inhibitor, as well as the possibility that these prodrugs are transformed into more than one inhibitor in bacteria. We also report that the onset of the potentiators is rapid. Their low cell cytotoxicity, good stability, and potentiation of various aminoglycosides, against both Gram-positive and Gram-negative bacteria, make them interesting compounds for the development of new drugs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acetiltransferases / Pró-Fármacos / Enterococcus faecium / Farmacorresistência Bacteriana / Escherichia coli / Antibacterianos Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Acetiltransferases / Pró-Fármacos / Enterococcus faecium / Farmacorresistência Bacteriana / Escherichia coli / Antibacterianos Limite: Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article