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Pancuronium bromide

CAS No. 15500-66-0

Pancuronium bromide ( NSC 293162 )

产品货号. M12200 CAS No. 15500-66-0

Pancurium dibromide 是一种竞争性 AChR 拮抗剂 (IC50 = 5.5 nM),可作为骨骼肌松弛剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
25MG ¥105 有现货
50MG ¥138 有现货
100MG ¥178 有现货
500MG ¥413 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥212 有现货

生物学信息

  • 产品名称
    Pancuronium bromide
  • 注意事项
    本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
  • 产品简述
    Pancurium dibromide 是一种竞争性 AChR 拮抗剂 (IC50 = 5.5 nM),可作为骨骼肌松弛剂。
  • 产品描述
    Pancuronium dibromide is a competitive AChR antagonist (IC50 = 5.5 nM) and acts as a skeletal muscle relaxant. Pancuronium dibromide interrupts neuromuscular transmission by competing with acetylcholine for receptor sites on the motor end-plate. (In Vitro):The action of Pancuronium on transmembrane sodium conductance is investigated in dorsal root ganglion neurones of chick embryos. Externally perfused Pancuronium (50 μM to 1 mM) reversibly inhibits the current by a fast mechanism of action. Inhibition is concentration-dependent (with a half-effective dose of 170 μM) but not voltage-dependent. Pancuronium may reduce the sodium current by interacting with the sodium channels in both the resting and open states.(In Vivo):Pancuronium (0.5 mg/kg; intravenous injection) abolishes the bradycardia induced both by injected acetylcholine (ACh) and by vagal nerve stimulation in guinea-pigs (250-300 g, male). At doses which produce 100% neuromuscular blockade, Pancuronium (0.04 mg/kg) potentiates vagally-induced bronchoconstriction.Potentiation by Pancuronium of the effects of adrenergic nerve stimulation, is found in rat anococcygeus and vas deferens.
  • 体外实验
    The action of Pancuronium on transmembrane sodium conductance is investigated in dorsal root ganglion neurones of chick embryos. Externally perfused Pancuronium (50 μM to 1 mM) reversibly inhibits the current by a fast mechanism of action. Inhibition is concentration-dependent (with a half-effective dose of 170 μM) but not voltage-dependent. Pancuronium may reduce the sodium current by interacting with the sodium channels in both the resting and open states.
  • 体内实验
    Pancuronium (0.5 mg/kg; intravenous injection) abolishes the bradycardia induced both by injected acetylcholine (ACh) and by vagal nerve stimulation in guinea-pigs (250-300 g, male). At doses which produce 100% neuromuscular blockade, Pancuronium (0.04 mg/kg) potentiates vagally-induced bronchoconstriction. Potentiation by Pancuronium of the effects of adrenergic nerve stimulation, is found in rat anococcygeus and vas deferens.
  • 同义词
    NSC 293162
  • 通路
    Endocrinology/Hormones
  • 靶点
    AChR
  • 受体
    AChR| mAChR
  • 研究领域
    Neurological Disease
  • 适应症
    ——

化学信息

  • CAS Number
    15500-66-0
  • 分子量
    732.67
  • 分子式
    C35H60Br2N2O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    Very soluble in water
  • SMILES
    CC(=O)O[C@H]1C[C@@H]2CC[C@@H]3[C@@H]([C@]2(C[C@@H]1[N+]4(CCCCC4)C)C)CC[C@]5([C@H]3C[C@@H]([C@@H]5OC(=O)C)[N+]6(CCCCC6)C)C.[Br-].[Br-]
  • 化学全称
    ——

运输与储存

  • 储存条件
    (-20℃)
  • 运输条件
    With Ice Pack
  • 稳定性
    ≥ 2 years

参考文献

1.Stovner J, et al. Br J Anaesth. 1975 Sep;47(9):949-54.
产品手册
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