Richardson K, Brammer K W, Marriott M S, Troke P F
Antimicrob Agents Chemother. 1985 May;27(5):832-5. doi: 10.1128/AAC.27.5.832.
The therapeutic potential of UK-49,858, a difluorophenyl bis-triazole derivative, has been assessed by evaluating its activity against systemic infections with Candida albicans in normal mice and rats and in mice with impaired defence mechanisms, against vaginal infections with C. albicans in mice, and against dermal infections with Trichophyton mentagrophytes in guinea pigs. Orally administered ketoconazole was used as a comparative agent throughout, and parenterally administered amphotericin B was included in the study of C. albicans systemic infection in normal mice. The activity of UK-49,858 given orally to mice or rats infected systemically with C. albicans was far superior to that of ketoconazole. In addition, UK-49,858 showed activity comparable to that of amphotericin B when given parenterally, although the latter gave more prolonged protection. UK-49,858 was also effective orally in curing experimental candidal vaginitis in mice and trichophytosis in guinea pigs, against which it was approximately 10 times more active than ketoconazole. These data suggest that UK-49,858 may be of value in the treatment of both C. albicans and dermatophyte fungal infections in man.
已通过评估 UK-49,858(一种二氟苯基双三唑衍生物)对正常小鼠和大鼠以及防御机制受损小鼠的白色念珠菌全身感染、对小鼠白色念珠菌阴道感染以及对豚鼠须癣毛癣菌皮肤感染的活性,来评估其治疗潜力。在整个实验过程中,口服酮康唑作为对照药物,在正常小鼠白色念珠菌全身感染研究中还加入了静脉注射两性霉素 B。口服 UK-49,858 对全身感染白色念珠菌的小鼠或大鼠的活性远优于酮康唑。此外,静脉注射时 UK-49,858 显示出与两性霉素 B 相当的活性,尽管后者提供的保护时间更长。UK-49,858 口服对小鼠实验性念珠菌性阴道炎和豚鼠癣病也有效,其活性比酮康唑高约 10 倍。这些数据表明,UK-49,858 可能对治疗人类白色念珠菌和皮肤癣菌真菌感染有价值。