Abstract
We investigated the activity of a pyrazolo-isothiazole derivative (G8) against Cryptococcus neoformans. A first screening test showed that G8 at 10 mg/L inhibited the growth of 14 of 15 clinical isolates tested. Killing experiments showed that fungicidal activity was achieved after 8 h of treatment with G8 at concentrations ≥10 mg/L. In a murine model of systemic cryptococcosis, G8 was effective at prolonging survival compared with the controls. Our data indicate that this new derivative has a potential therapeutic role in infections caused by C. neoformans.
Cite
CITATION STYLE
Barchiesi, F., Milici, M. E., Arzeni, D., Schimizzi, A. M., Pizzo, G., Giammanco, G. M., … Vicentini, C. B. (2003). In vitro and in vivo anticryptococcal activities of a new pyrazolo-isothiazole derivative. Journal of Antimicrobial Chemotherapy, 51(1), 167–170. https://doi.org/10.1093/jac/dkg019
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.