一种新的口服活性烯丙胺衍生物SF 86-327的体外研究。

S Shadomy, A Espinel-Ingroff, R J Gebhart
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引用次数: 113

摘要

SF 86-327 (Sandoz Forschungsinstitut)是一种与naftifine相关的口服活性烯丙胺衍生物。用琼脂稀释法比较SF 86-327与萘替芬、酮康唑和伊曲康唑(R 51,211, Janssen pharma)的体外抑菌活性。共分离了120株真菌。采用肉汤稀释法测定了SF 86-327和naftifine对18种二态病原菌的体外抑菌活性。这些研究结果支持SF 86-327是一种广谱抗真菌剂的说法。肉汤稀释试验结果还显示,SF 86-327在体外对皮炎芽孢菌、荚膜组织浆菌和申克孢子丝菌具有抑菌和杀菌作用,浓度低至0.05微克ml-1(18株菌株MIC90 = 0.39微克ml-1, MFC90 = 12.5微克ml-1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In-vitro studies with SF 86-327, a new orally active allylamine derivative.

SF 86-327 (Sandoz Forschungsinstitut) is an orally active allylamine derivative related to naftifine. The antifungal activity of SF 86-327 was compared in vitro with those of naftifine, ketoconazole, and itraconazole (R 51,211, Janssen Pharmaceutica) by agar dilution. 120 fungal isolates were tested. Also, the antifungal activities of SF 86-327 and naftifine against 18 dimorphic pathogens were assayed in vitro by broth dilution. Results of these studies support claims that SF 86-327 is a broad spectrum antifungal agent. Results of the broth dilution studies also revealed that SF 86-327 was both fungistatic and fungicidal in vitro for isolates of Blastomyces dermatitidis, Histoplasma capsulatum and Sporothrix schenckii at concentrations as low as 0.05 micrograms ml-1 (18 isolates tested, MIC90 = 0.39 micrograms ml-1, MFC90 = 12.5 micrograms ml-1).

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