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A representative of arylcyanomethylenequinone oximes effectively inhibits growth and formation of hyphae in Candida albicans and influences the activity of protein kinases in vitro
Authors:Maciej Masłyk  Monika Janeczko  Oleg M. Demchuk  Anna Boguszewska-Czubara  Hieronim Golczyk  Anna Sierosławska  Anna Rymuszka  Aleksandra Martyna  Konrad Kubiński
Affiliation:1. Department of Molecular Biology, Institute of Biotechnology, The John Paul II Catholic University of Lublin, ul. Konstantynów 1i, 20-708 Lublin, Poland;2. Organic Chemistry Department, Faculty of Chemistry, Maria Curie-Sk?odowska University, ul. Gliniana 33, 20-614 Lublin, Poland;3. Department of Medical Chemistry, Medical University of Lublin, ul. Chod?ki 4A, 20-093 Lublin, Poland;4. Department of Animal Physiology and Toxicology, Institute of Biotechnology, The John Paul II Catholic University of Lublin, ul. Konstantynów 1i, 20-708 Lublin, Poland
Abstract:In this study, we applied various assays to reveal new activities of phenylcyanomethylenequinone oxime-4-(hydroxyimino) cyclohexa-2,5-dien-1-ylidene](phenyl)ethanenitrile (4-AN) for potential anti-microbial applications. These assays demonstrated (a) the antimicrobial effect on bacterial and fungal cultures, (b) the effect on the in vitro activity of the kinase CK2, (c) toxicity towards human erythrocytes, the Caco-2 cancer cell line, and embryonic development of Zebrafish. We demonstrated the activity of 4-AN against selected bacteria and Candida spp. The MIC ranging from 4?µg/ml to 125?µg/ml proved effective in inhibition of formation of hyphae and cell aggregation in Candida, which was demonstrated at the cytological level. Noteworthy, 4-AN was found to inhibit the CK2 kinase with moderate potency. Moreover, at low concentrations, it did not exert any evident toxic effects on human erythrocytes, Caco-2 cells, or Zebrafish embryos. 4-AN can be a potential candidate as a novel drug against Candida infections.
Keywords:Arylcyanomethylenequinone oximes  Antifungal agents  Hyphae  Phosphorylation
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