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In-vitro studies of two 5-nitroimidazole derivatives.
Castelli, M; Malagoli, M; Ruberto, A I; Baggio, A; Casolari, C; Cermelli, C; Bossa, M R; Rossi, T; Paolucci, F; Roffia, S.
Afiliación
  • Castelli M; Department of Biomedical Sciences, Section of Pharmacology, University of Modena, Italy.
J Antimicrob Chemother ; 40(1): 19-25, 1997 Jul.
Article en En | MEDLINE | ID: mdl-9249200
ABSTRACT
This paper reports the findings obtained using two new compounds belonging to the 5-nitroimidazole family sulphuridazole (V1) and sulphonidazole (V2). We first assessed their antimicrobial activity on Clostridia spp. and then extended the study to Gram-positive and Gram-negative aerobic microorganisms and to Candida albicans. Their MICs were compared with those of metronidazole. The findings show that the antibacterial and antimycotic activity of sulphonidazole is greater than that of sulphuridazole, while metronidazole is not active against any aerobic organism. It also emerges that the NO2 group is indispensable for all the microorganisms assayed and that sulphuridazole and sulphonidazole are the first two 5-nitroimidazoles active against C. albicans. The redox potentials of the 5-nitroimidozoles studied suggest that their action mechanism is mainly based on redox processes.
Asunto(s)
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Base de datos: MEDLINE Asunto principal: Sulfonas / Bacterias / Antiinfecciosos / Nitroimidazoles Idioma: En Revista: J Antimicrob Chemother Año: 1997 Tipo del documento: Article
Buscar en Google
Base de datos: MEDLINE Asunto principal: Sulfonas / Bacterias / Antiinfecciosos / Nitroimidazoles Idioma: En Revista: J Antimicrob Chemother Año: 1997 Tipo del documento: Article