一种新型3-氨甲基利福霉素的抗菌活性。

Il Farmaco; edizione scientifica Pub Date : 1988-07-01
V Strippoli, T Bruzzese, R Galli, N Simonetti, N Tronci
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引用次数: 0

摘要

新的3-氨甲基利福霉素SPA-S-565在体外具有与利福平相当的抗菌活性。事实上,SPA-S-565对多种葡萄球菌和链球菌属革兰氏阳性球菌以及20株结核分枝杆菌的抗菌活性与利福平相似。在腹腔感染金黄色葡萄球菌牛津株或化脓性链球菌的瑞士白化病小鼠中,SPA-S-565和利福平的保护作用相当显著,两种抗生素之间无显著差异。在每7天给药一次的结核分枝杆菌感染小鼠中,SPA-S-565的保护作用明显大于利福平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The antibacterial activity of a new 3-azinomethyl-rifamycin.

The new 3-azinomethyl-rifamycin, SPA-S-565, was shown to exert an effective antibacterial activity in vitro comparable to that of rifampicin. In fact, the antibacterial activity of SPA-S-565 against numerous Gram-positive cocci belonging to Staphylococcus and Streptococcus species as well as against 20 strains of Mycobacterium tuberculosis, was similar to that of rifampicin. In Swiss albino mice intraperitoneally infected with Staphylococcus aureus Oxford strain or Streptococcus pyogenes, the protective activity of SPA-S-565 and rifampicin was quite remarkable, and no significant difference was noted between the two antibiotics. In M. tuberculosis-infected mice treated with the antibacterial agents every seven days, the protection exerted by SPA-S-565 was significantly greater than that exerted by rifampicin.

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