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Munster Technological University

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In vitro cytotoxicity

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Full-Text Articles in Bacterial Infections and Mycoses

Antimycobacterial And Photosynthetic Electron Transport Inhibiting Activity Of Ring-Substituted 4-Arylamino-7-Chloroquinolinium Chlorides, Jan Otrevel, Pavel Bobal, Iveta Zadrazilova, Rodeney Govender, Matus Pesko, Stanislava Keltosova, Petra Koleckarova, Petr Marsalek, Ales Imramovsky, Aidan Coffey, Jim O'Mahony, Peter Kollar, Alois Cizek, Katarina Kralova, Josef Jampilek Sep 2013

Antimycobacterial And Photosynthetic Electron Transport Inhibiting Activity Of Ring-Substituted 4-Arylamino-7-Chloroquinolinium Chlorides, Jan Otrevel, Pavel Bobal, Iveta Zadrazilova, Rodeney Govender, Matus Pesko, Stanislava Keltosova, Petra Koleckarova, Petr Marsalek, Ales Imramovsky, Aidan Coffey, Jim O'Mahony, Peter Kollar, Alois Cizek, Katarina Kralova, Josef Jampilek

Department of Biological Sciences Publications

In this study, a series of twenty-five ring-substituted 4-arylamino-7-chloroquinolinium chlorides were prepared and characterized. The compounds were tested for their activity related to inhibition of photosynthetic electron transport (PET) in spinach (Spinacia oleracea L.) chloroplasts and also primary in vitro screening of the synthesized compounds was performed against mycobacterial species. 4-[(2-Bromophenyl)amino]-7-chloroquinolinium chloride showed high biological activity against M. marinum, M. kansasii, M. smegmatis and 7-chloro-4-[(2-methylphenyl)amino]quinolinium chloride demonstrated noteworthy biological activity against M. smegmatis and M. avium subsp. paratuberculosis. The most effective compounds demonstrated quite low toxicity (LD50 > 20 μmol/L) against the human monocytic leukemia THP-1 cell line within preliminary …