A Novel Series of Acylhydrazones as Potential Anti- Candida Agents: Design, Synthesis, Biological Evaluation and In Silico Studies

Molecules. 2019 Jan 6;24(1):184. doi: 10.3390/molecules24010184.

Abstract

In the context of an increased incidence of invasive fungal diseases, there is an imperative need of new antifungal drugs with improved activity and safety profiles. A novel series of acylhydrazones bearing a 1,4-phenylene-bisthiazole scaffold was designed based on an analysis of structures known to possess anti-Candida activity obtained from a literature review. Nine final compounds were synthesized and evaluated in vitro for their inhibitory activity against various strains of Candida spp. The anti-Candida activity assay revealed that some of the new compounds are as active as fluconazole against most of the tested strains. A molecular docking study was conducted in order to evaluate the binding poses towards lanosterol 14α-demethylase. An in silico ADMET analysis showed that the compounds possess drug-like properties and represent a biologically active framework that should be further optimized as potential hits.

Keywords: ADMET; acylhydrazone; anti-Candida; lanosterol 14α-demethylase; molecular modeling; thiazole.

MeSH terms

  • Antifungal Agents / chemical synthesis
  • Antifungal Agents / pharmacology*
  • Candida / drug effects*
  • Drug Design
  • Fluconazole / pharmacology
  • Hydrazones / chemical synthesis
  • Hydrazones / pharmacology*
  • Microbial Sensitivity Tests
  • Molecular Docking Simulation
  • Molecular Structure
  • Protein Binding
  • Structure-Activity Relationship

Substances

  • Antifungal Agents
  • Hydrazones
  • Fluconazole