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ZONIPORIDE DIHYDROCHLORIDE

ZONIPORIDE DIHYDROCHLORIDE,241800-97-5,结构式
ZONIPORIDE DIHYDROCHLORIDE
  • CAS号:241800-97-5
  • 英文名:ZONIPORIDE DIHYDROCHLORIDE
  • 中文名:ZONIPORIDE DIHYDROCHLORIDE
  • CBNumber:CB12453438
  • 分子式:C17H17ClN6O
  • 分子量:356.81
  • MOL File:241800-97-5.mol
ZONIPORIDE DIHYDROCHLORIDE化学性质
  • 储存条件 :Desiccate at -20°C
  • 溶解度 :≤1mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in dimethyl formamide
  • 形态 :crystalline solid
  • 稳定性 :Hygroscopic

ZONIPORIDE DIHYDROCHLORIDE性质、用途与生产工艺

  • 生物活性 Zoniporide (CP-597396) hydrochloride 是 1 型钠氢交换剂 (NHE-1) 的有效和选择性抑制剂。Zoniporide hydrochloride 抑制人 NHE-1 (IC50=14 nM),与其他 NHE 亚型相比具有大于 150 倍的选择性,并有效抑制离体 NHE-1 依赖性的人血小板溶胀 (IC50=59 nM)。
  • 靶点

    IC50: 14 nM (NHE-1)

  • 体内研究

    Zoniporide (0.25-4 mg/kg; i.v.; every hour for 2 hours) elicits a dose-dependent reduction in infarct size (ED 50 =0.45 mg/kg/h) in open chest anesthetized rabbits.
    Zoniporide exhibits moderate plasma protein binding, has a t 1/2 of 1.5 hours in monkeys, and has one major active metabolite.
    Zoniporide treatment shows the AUC 0-∞ and t 1/2 are 0.07 μg h/mL and 0.5 hours, respectively.

    Animal Model: Rabbit
    Dosage: 0.25, 1, 4 mg/kg
    Administration: Every hour for 2 hours; intravenous injection
    Result: Elicited a significant dose-dependent reduction in infarct size in the anesthetized rabbit. The ED 50 was 0.45 mg/kg/h.
    Animal Model: Rat
    Dosage: 1 mg/kg
    Administration: Intravenous injection(Pharmacokinetic Analysis)
    Result: The AUC 0-∞ and t 1/2 were 0.07 μg h/mL and 0.5 hours, respectively.
ZONIPORIDE DIHYDROCHLORIDE上下游产品信息
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ZONIPORIDE DIHYDROCHLORIDE生产厂家
  • 公司名称:VDM Biochemicals
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