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Exploring Structure-Activity Relationships of Niclosamide-Based Colistin Potentiators in Colistin-Resistant Gram-Negative Bacteria.
Berry, Liam; Neale, Quinn; Arora, Rajat; Ramirez, Danyel; Brizuela, Marc; Domalaon, Ronald; Arthur, Gilbert; Schweizer, Frank.
Afiliação
  • Berry L; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Neale Q; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Arora R; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Ramirez D; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Brizuela M; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Domalaon R; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
  • Arthur G; Department of Biochemistry and Medical Genetics, University of Manitoba, Winnipeg, MB R3E 3N4, Canada.
  • Schweizer F; Department of Chemistry, University of Manitoba, Winnipeg, MB R3T 2N2, Canada.
Antibiotics (Basel) ; 13(1)2024 Jan 03.
Article em En | MEDLINE | ID: mdl-38247602
ABSTRACT
Colistin is primarily used as a last resort antibiotic against highly resistant Gram-negative bacteria (GNB). Rising rates of colistin resistance, however, may limit future use of this agent. The anthelmintic drug niclosamide has been shown to enhance colistin activity in combination therapy, but a detailed structure-activity relationship (SAR) for niclosamide against GNB has yet to be studied. A series of niclosamide analogs were synthesized to perform an SAR, leading to the discovery of a lead compound that displayed comparable colistin-potentiating activity to niclosamide with reduced cytotoxicity. Overall, this work provides important insights into synthetic strategies for the future development of new niclosamide derivatives and demonstrates that toxicity to mammalian cells can be reduced while maintaining colistin potentiation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article