New Chalcone-Triazole Hybrids with Promising Antimicrobial Activity in Multidrug Resistance Strains

• Tipo: Artigo em Revista Científica Internacional
• Data: 2022

Autores

Pereira, D (Autor) Outra; Duraes, F (Autor) Outra; Szemeredi, N (Autor) Outra; Freitas-da-Silva, J (Autor) Outra; Eugenia Pinto (Autor) FFUP; Martins-da-Costa, P (Autor) Outra; Pinto, M (Autor) Outra; Marta Correia da Silva (Autor) FFUP; Spengler, G (Autor) Outra; Emilia Sousa (Autor) FFUP; Honorina Cidade (Autor) FFUP

Revista

Título: International Journal Of Molecular Sciences

Vol. 23

ISSN: 1661-6596

Editora: MDPI

Indexação

ISI Web of Knowledge - 8 Citações

Scopus - 8 Citações

Outras Informações

ID Authenticus: P-00X-G13

DOI: 10.3390/ijms232214291

Abstract (EN): Resistance to antibiotics is an emerging problem worldwide, which leads to an increase in morbidity and mortality rates. Several mechanisms are attributed to bacterial resistance, overexpression of efflux pumps being one of the most prominent. As an attempt to develop new effective antimicrobial drugs, which could be able to act against resistant bacterial strains and considering the antimicrobial potential of flavonoids and triazolyl flavonoid derivatives, in particular chalcones, a small library of chalcone derivatives was synthesized and evaluated for its potential to act as antimicrobials and/or adjuvants in combination with antibiotics towards resistant bacteria. Although only compound 7 was able to act as antibacterial, compounds 1, 2, 4, 5, 7, and 9 revealed to be able to potentiate the activity of antibiotics in resistant bacteria. Moreover, five compounds (3, 5-8) demonstrated to be effective inhibitors of efflux pumps in Salmonella enterica serovar Typhimurium SL1344, and four compounds (1, 3, 7, and 10) showed higher ability than reserpine to inhibit biofilm formation of resistant Staphylococcus aureus 272123. Together, our results showed the potential of these compounds regarding reversion of bacterial resistance.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 18