4.6 Article

New Nitrogen Compounds Coupled to Phenolic Units with Antioxidant and Antifungal Activities: Synthesis and Structure-Activity Relationship

Journal

MOLECULES
Volume 23, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/molecules23102530

Keywords

Imidazoles; phenolic compounds; antifungal activity; MIC; antioxidant capacity; structure-activity relationship

Funding

  1. Portuguese Fundacao para a Ciencia e Tecnologia [PPCDT/QUI/59356]
  2. Portuguese FCT [SFRH/BPD/26106]

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A selection of 1-amino-2-arylidenamine-1,2-(dicyano)ethenes 3 was synthesized and cyclized to 2-aryl-4,5-dicyano-1H-imidazoles 4 upon reflux in ethyl acetate/acetonitrile, in the presence of manganese dioxide. These compounds were tested for their antioxidant capacity by cyclic voltammetry, 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical and deoxyribose degradation assays. The minimum inhibitory concentration of all compounds was evaluated against two yeast species, Saccharomyces cerevisiae and Candida albicans. Their toxicity was tested in mammal fibroblasts. Among the synthesised compounds, two presented dual antioxidant/antifungal activity without toxic effects in fibroblasts. The new compounds synthesized in this work are potential biochemical tools and/or therapeutic drugs.

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