Abstract
Some new 2-aryl-4-quinazolinone derivatives bearing a cyclic amino group at position 6 were prepared and their preliminary cytotoxic and antifungal evaluation is reported. They all showed a moderate cytotoxicity suggesting that not only the oxidation state of the N1-C2 bond is a crucial factor for this kind of biological activity. These quinazolinones were tested against several yeast, filamentous and dermatophyte fungi showing all to be inactive.
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CITATION STYLE
López, S. E., Rosales, M. E., Canelón, C. E., Valverde, E. A., Narváez, R. C., Charris, J. E., … Zacchino, S. (2001). Synthesis and preliminary cytotoxic and antifungal evaluation of some 6-N,N-dialkyl 2-aryl-4(3H)-quinazolinone derivatives. Heterocyclic Communications, 7(5), 473–480. https://doi.org/10.1515/HC.2001.7.5.473
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