Tetrazole hybrids and their antifungal activities

Eur J Med Chem. 2019 May 15:170:225-234. doi: 10.1016/j.ejmech.2019.03.023. Epub 2019 Mar 15.

Abstract

Fungi, which can cause serious infections, results in more than 1.35 million deaths annually throughout the world. Azole antifungal drugs which could inhibit the enzyme lanosterol 14α-demethylase, occupy an important position in the treatment of fungal infections. Tetrazoles, practically non-metabolized bioisosteric analog of carboxylic acid and cis-amide, possess a variety of chemotherapeutic properties, including antifungal activities. Hybridization represents a promising strategy to develop novel drugs, and hybridization of tetrazole with other antifungal pharmacophores has the potential to increase the activity and overcome the drug resistance. Various tetrazole hybrids have been designed, synthesized and screened for their antifungal activities, and some of them showed promising activity against both drug-susceptible and drug-resistant fungi. In this review, we present tetrazole hybrids for fighting against fungi. The structure-activity relationship (SAR) is also discussed to provide an insight for rational designs of more effective candidates.

Keywords: Antifungal activity; Fungi; Hybrid compounds; Structure-activity relationship; Tetrazole.

Publication types

  • Review

MeSH terms

  • Animals
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology*
  • Azoles / chemistry
  • Azoles / pharmacology
  • Fungi / drug effects*
  • Humans
  • Mycoses / drug therapy
  • Pyridines / chemistry
  • Pyridines / pharmacology
  • Pyrimidines / chemistry
  • Pyrimidines / pharmacology
  • Quinolines / chemistry
  • Quinolines / pharmacology
  • Structure-Activity Relationship
  • Tetrazoles / chemistry*
  • Tetrazoles / pharmacology*

Substances

  • Antifungal Agents
  • Azoles
  • Pyridines
  • Pyrimidines
  • Quinolines
  • Tetrazoles
  • 1H-tetrazole