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CAS No. : 86386-73-4
MCE 国际站:Fluconazole
产品活性:Fluconazole (UK-49858) 是一种三唑类抗真菌剂 (antifungal),对多种真菌具有优异的活性,尤其对Candida albicans,Fluconazole 抑制C. albicans 和 Candida kefyr 的 IC99 为 0.20 μg/mL 至 0.39 μg/mL。
研究领域:Anti-infection
作用靶点:Fungal | Antibiotic | Bacterial
In Vitro: Fluconazole inhibits 4 species ofAspergillus fumigatus with the IC50s of 23.9-43.5 μg/mL. Fluconazole (0.20 μg/mL) inhibits significantly the mycelial-phase growth and germ tube elongation of C. albicans in a medium supplemented with serum.
Fluconazole is a triazole antifungal agent that has been available for the treatment of infections due to Candida, Cryptococcus. The MIC90 is highest for C. krusei (MIC ≥ 64 μg/mL) and C. glabrata (MIC, 32 μg/mL) and is ≤2 μg/mL for C. albicans (0.5 μg/mL), C. parapsilosis (2 μg/mL), C. tropicalis (2 μg/mL), C. lusitaniae (2 μg/mL), and C. kefyr (0.5 μg/mL).
Fluconazole (0.1-50.0 μg/mL) damages the fungal cells and reduces their viability.
In Vivo: Fluconazole ( 0, 0.5, 1, 2.5, 5, 7.5, and 10 mg/kg; administered intraperitoneally (i.p.) as a single dose) results in a 50% reduction in fungal densities (ED50) of 4.87 mg/kg in a murine model of systemic candidiasis. ?Fluconazole exhibits terminal elimination half-life of 2.4 h) following i.p. administration.The terminal half-life does not change with the dose of fluconazole administered.
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