In-vitro studies of two 5-nitroimidazole derivatives

被引:17
作者
Castelli, M
Malagoli, M
Ruberto, AI
Baggio, A
Casolari, C
Cermelli, C
Bossa, MR
Rossi, T
Paolucci, F
Roffia, S
机构
[1] UNIV MODENA,DEPT BIOMED SCI,SECT HYG & MICROBIOL,I-41100 MODENA,ITALY
[2] UNIV MILAN,DEPT PHARMACOL CHEMOTHERAPY & MED TOXICOL,MILAN,ITALY
[3] UNIV MODENA,DEPT PHARMACEUT SCI,I-41100 MODENA,ITALY
[4] UNIV BOLOGNA,DEPT CHEM G CIAMICIAN,BOLOGNA,ITALY
关键词
D O I
10.1093/jac/40.1.19
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 NO, 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.
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页码:19 / 25
页数:7
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