Derivatives of Trimethoxybenzoic Acid and Gallic Acid as Potential Efflux Pump Inhibitors In Silico and In Vitro Studies /

The overexpression of efflux pumps is one of the strategies used by bacteria to resist antibiotics and could be targeted to circumvent the antibiotic crisis. In this work, a series of trimethoxybenzoic acid derivatives previously described as antifouling compounds was explored for potential antimicr...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Neves Ana Rita
Durães Fernando
Freitas-Silva Joana
Szemerédi Nikoletta
Martins-da-Costa Paulo
Pinto Eugénia
Correia-da-Silva Marta
Spengler Gabriella
Sousa Emília
Dokumentumtípus: Cikk
Megjelent: 2022
Sorozat:INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 23 No. 22
Tárgyszavak:
doi:10.3390/ijms232214468

mtmt:33288701
Online Access:http://publicatio.bibl.u-szeged.hu/25689
Leíró adatok
Tartalmi kivonat:The overexpression of efflux pumps is one of the strategies used by bacteria to resist antibiotics and could be targeted to circumvent the antibiotic crisis. In this work, a series of trimethoxybenzoic acid derivatives previously described as antifouling compounds was explored for potential antimicrobial activity and efflux pump (EP) inhibition. First, docking studies on the acridine resistance proteins A and B coupled to the outer membrane channel TolC (AcrAB-TolC) efflux system and a homology model of the quinolone resistance protein NorA EP were performed on 11 potential bioactive trimethoxybenzoic acid and gallic acid derivatives. The synthesis of one new trimethoxybenzoic acid derivative (derivative 13) was accomplished. To investigate the potential of this series of 11 derivatives as antimicrobial agents, and in reverting drug resistance, the minimum inhibitory concentration was determined on several strains (bacteria and fungi), and synergy with antibiotics and EP inhibition were investigated. Derivative 10 showed antibacterial activity against the studied strains, derivatives 5 and 6 showed the ability to inhibit EPs in the acrA gene inactivated mutant Salmonella enterica serovar Typhimurium SL1344, and 6 also inhibited EPs in Staphylococcus aureus 272123. Structure-activity relationships highlighted trimethoxybenzoic acid as important for EP inhibitory activity. Although further studies are necessary, these results show the potential of simple trimethoxybenzoic acid derivatives as a source of feasible EP inhibitors.
Terjedelem/Fizikai jellemzők:15
ISSN:1661-6596