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S84196

Fosfluconazole

源叶(MedMol) 99%
  • 英文名:
  • Fosfluconazole
  • 别名:
  • 2-(2,4-二氟苯基)-1,3-二(1H-1,2,4-三氮唑-1-基)丙基二氢磷酸酯;磷康唑;福司氟康唑;磷氟康唑(福司氟康唑);磷氟康唑;2-(2,4-difluorophenyl)-1,3-di(1H-1,2,4-triazol-1-yl)propyl dihydrogen phosphate;Prodif
  • CAS号:
  • 194798-83-9
  • 分子式:
  • C13H13F2N6O4P
  • 分子量:
  • 386.251
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源叶(MedMol) S84196-10mg 99% ¥406.00元 10 - - - EA 加入购物车
源叶(MedMol) S84196-25mg 99% ¥895.00元 6 - - - EA 加入购物车
源叶(MedMol) S84196-100mg 99% ¥2470.00元 2 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Fosfluconazole is water-soluble phosphate prodrug of fluconazole. Fluconazole is an antifungal drug.
  • 靶点: Antifungal
  • 体内研究:
    Fosfluconazole was administered intravenously and intraperitoneally. After the i.p. administration of F-FLCZ, FLCZ was detected in circulating blood and the dialyzing fluid in peritoneal dialysis rats. The concentration of plasma FLCZ after the i.p. F-FLCZ administration was lower than that after the intravenous (i.v.) F-FLCZ administration
  • 动物实验: Twelve-week-old male Wistar rats (200–300 g) were used. They were housed in a temperature-controlled room and were given food and water ad libitum. All rats were anesthetized by an i.p. administration of pentobarbital (50 mg/kg body weight). A catheter was placed in the peritoneal cavity and used as an inflow drain for the dialyzing fluid. sampling. In rats receiving i.v. administration, a catheter was inserted into the left jugular vein for drug administration, and another into the right femoral artery for blood sampling. Blood samples after the i.p. administration were obtained from the heart. The rats were then allowed to recover from the anesthesia and surgery for at least 24 hr. After the 40-mL dialyzing fluid was administered intraperitoneally, FLCZ 16 mg/kg body weight) and F-FLCZ (16 mg FLCZ eq/kg body weight) were administered intravenously. The volume of the drug solution administered intravenously was 8 mL/kg. FLCZ (16 mg/kg body weight) and F-FLCZ (16 mg FLCZ eq/kg body weight) dissolved in the 40
  • 参考文献:
    1. Aoyama T, et al. Pharmacokinetics of fluconazole and Fosfluconazole after intraperitoneal administration to peritoneal dialysis rats. Drug Metab Pharmacokinet. 2005 Dec;20(6):485-90. 2. Yuan H, et al. Evaluation of in vitro models for screening alkaline phosphatase-mediated bioconversion of phosphate ester prodrugs. Drug Metab Dispos. 2009 Jul;37(7):1443-7.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.589 ml 12.945 ml 25.89 ml
    5 mM 0.518 ml 2.589 ml 5.178 ml
    10 mM 0.259 ml 1.294 ml 2.589 ml
    50 mM 0.052 ml 0.259 ml 0.518 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)


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