| Literature DB >> 27795371 |
Hamed Fakhim1,2, Saeed Emami3, Afsane Vaezi1,2, Seyedeh Mahdieh Hashemi3, Leila Faeli1,2, Kambiz Diba4, Eric Dannaoui5, Hamid Badali6,7.
Abstract
The in vitro activities of two novel azole compounds (aryl-1,2,4-triazol-3-ylthio analogues of fluconazole [ATTAFs]) and five comparator antifungal agents against 52 clinical Candida isolates from 5 different species were determined. The novel azole compounds had the lowest geometric mean MICs, followed by fluconazole. Moreover, combinations of these compounds with fluconazole exhibited synergistic effects against fluconazole-susceptible (22 of 23 isolates), fluconazole-susceptible dose-dependent (10 of 13 isolates), and fluconazole-resistant (1 of 16 isolates) Candida isolates.Entities:
Keywords: Candida species; In vitro susceptibility; triazole derivatives
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Year: 2016 PMID: 27795371 PMCID: PMC5192144 DOI: 10.1128/AAC.01106-16
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191