Abstract
Different N-substituted benzisoselenazol-3(2H)-ones, analogues of ebselen were designed as new antiviral and antimicrobial agents. We report their synthesis, chemical properties as well as study on biological activity against broad spectrum of pathogenic microorganisms (Staphylococcus aureus, Staphylococcus simulans, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Candida albicans, Aspergillus niger) and viruses (herpes simplex virus type 1 (HSV-1), encephalomyocarditis virus (EMCV), vesicular stomatitis virus (VSV)), in vitro. Most of them exhibited high activity against viruses (HSV-1, EMCV) and gram-positive bacteria strains (S. aureus, S. simulans), while their activity against gram-negative bacteria strains (E. coli, P. aeruginosa, K. pneumoniae) was substantially lower. Some of tested compounds were active against yeast C. albicans and filamentous fungus A. niger. © 2008 Pharmaceutical Society of Japan.
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Piȩtka-Ottlik, M., Wójtowicz-Młochowska, H., Kołodziejczyk, K., Piasecki, E., & Młochowski, J. (2008). New organoselenium compounds active against pathogenic bacteria, fungi and viruses. Chemical and Pharmaceutical Bulletin, 56(10), 1423–1427. https://doi.org/10.1248/cpb.56.1423
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