Quinazoline derivatives are efficient chemosensitizers of antibiotic activity in Enterobacter aerogenes, Klebsiella pneumoniae and Pseudomonas aeruginosa resistant strains.

J, Chevalier , A Mahamoud , M, Baitiche , E Adam , Miguel Viveiros Bettencourt, A, Smarandache , A, Militaru , ML, Pascu , Leonard Amaral, JM Pagès

Research output: Contribution to journalArticlepeer-review

43 Citations (Scopus)


Amongst the three series of quinazoline derivatives synthesised and studied in this work, some molecules increase the antibiotic susceptibility of Gram-negative bacteria presenting multidrug-resistant phenotypes. N-alkyl compounds induced an increase in the activity of chloramphenicol, nalidixic acid and sparfloxacin, which are substrates of the AcrAB-TolC and MexAB-OprM efflux pumps in clinical isolates. These molecules are able to increase the intracellular concentration of chloramphenicol in efflux pump-overproducing strains. Their activity depends on the antibiotic structure, suggesting that different sites may be involved for the recognition of substrates by a given efflux pump. Quinazoline molecules exhibiting a nitro functional group are more active, and structure-activity relationship studies may be undertaken to identify the pharmacophoric group involved in the AcrB and MexB affinity sites. (C) 2010 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.
Original languageEnglish
Pages (from-to)164-168
JournalInternational Journal Of Antimicrobial Agents
Issue number2
Publication statusPublished - 1 Jan 2010


Dive into the research topics of 'Quinazoline derivatives are efficient chemosensitizers of antibiotic activity in <em>Enterobacter</em> <em>aerogenes</em>, <em>Klebsiella pneumoniae</em> and <em>Pseudomonas aeruginosa</em> resistant strains.'. Together they form a unique fingerprint.

Cite this