In vitro activities of novel azole compounds ATTAF-1 and ATTAF-2 against fluconazole-susceptible and-resistant isolates of candida species

31Citations
Citations of this article
20Readers
Mendeley users who have this article in their library.

This article is free to access.

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.

Cite

CITATION STYLE

APA

Fakhim, H., Emami, S., Vaezi, A., Hashemi, S. M., Faeli, L., Diba, K., … Badali, H. (2017). In vitro activities of novel azole compounds ATTAF-1 and ATTAF-2 against fluconazole-susceptible and-resistant isolates of candida species. Antimicrobial Agents and Chemotherapy, 61(1). https://doi.org/10.1128/AAC.01106-16

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free