Current advances of triazole alcohols derived from fluconazole : Design, in vitro and in silico studies

Copyright © 2019 Elsevier Masson SAS. All rights reserved..

Currently, the available antifungal agents have significant clinical incompetency in terms of their clinical efficacy, antifungal spectrum, unfavorable pharmacokinetic profiles, substantial side effects and drug-drug interactions. Thus, the optimization and improvement of existing drugs and identification of new antifungal agents are urgently needed. Fluconazole is the first triazole alcohol drug with good in vivo efficacy against yeasts and well-known targets in fungal cells. However, the wide use of fluconazole as a first-line antifungal therapy has led to the development of resistance in clinical isolates of Candida species including Candida albicans and the emerging non-albicans Candida spp. In the last years, extensive efforts inflected to design and discovery of triazole alcohols derived from fluconazole by replacing one triazole ring with the proper side chain. In this paper, we have reviewed the structural modification of fluconazole to pursuit potent triazole alcohols with improved anti-Candida activity, and have highlighted their in vitro activities and in silico studies.

Medienart:

E-Artikel

Erscheinungsjahr:

2019

Erschienen:

2019

Enthalten in:

Zur Gesamtaufnahme - volume:170

Enthalten in:

European journal of medicinal chemistry - 170(2019) vom: 15. Mai, Seite 173-194

Sprache:

Englisch

Beteiligte Personen:

Emami, Saeed [VerfasserIn]
Ghobadi, Elham [VerfasserIn]
Saednia, Shahnaz [VerfasserIn]
Hashemi, Seyedeh Mahdieh [VerfasserIn]

Links:

Volltext

Themen:

8VZV102JFY
Antifungal Agents
Antifungal activity
Azole antifungals
Fluconazole
Journal Article
Lanosterol 14α-demethylase
Review
Triazoles

Anmerkungen:

Date Completed 19.04.2019

Date Revised 19.04.2019

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1016/j.ejmech.2019.03.020

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM295200200