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Vecuronium bromide

CAS No. 50700-72-6

Vecuronium bromide ( NC 45 )

产品货号. M14731 CAS No. 50700-72-6

维库溴铵(溴化物)是一种非去极化阻断剂类别的肌肉松弛剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥125 有现货
5MG ¥183 有现货
10MG ¥253 有现货
25MG ¥423 有现货
50MG ¥616 有现货
100MG ¥873 有现货
500MG ¥2142 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥265 有现货

生物学信息

  • 产品名称
    Vecuronium 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
    维库溴铵(溴化物)是一种非去极化阻断剂类别的肌肉松弛剂。
  • 产品描述
    Vecuronium (bromide) is a muscle relaxant in the category of non-depolarizing blocking agents.(In Vitro):Vecuronium bromide (0-100 μM, 15 min) inhibits [3H] norepinephrine (NE) uptake to 65% at 100 μM in adrenal medullary cells.Vecuronium bromide (0-15 μM,72 hours) inhibits cancer cell proliferation and migration in a concentration-dependent manner.Vecuronium bromide (0-15 μM,72 hours) can significantly reduce cell viability by combining with cisplatin.(In Vivo):Vecuronium bromide (Intravenous injection, 0-5 μM, every 30 min, 2 hours) attenuates the response of carotid sinus nerve activity (CSNA) to hypoxia in a dose-dependent manner and inhibits the neural response of the carotid body to acetylcholine (ACh) in Wister rats.
  • 体外实验
    Vecuronium bromide (0-100 μM, 15 min) inhibits [3H] norepinephrine (NE) uptake to 65% at 100 μM in adrenal medullary cells.Vecuronium bromide (0-15 μM,72 hours) inhibits cancer cell proliferation and migration in a concentration-dependent manner.Vecuronium bromide (0-15 μM,72 hours) can significantly reduce cell viability by combining with cisplatin.Cell Proliferation Assay Cell Line:Lung cancer cell line (A549)Concentration:0-15 μM Incubation Time:72 hours Result:Inhibited cell proliferation at concentrations ranging from 5.0 μM to 15 μM.Cell Cytotoxicity Assay Cell Line:Lung cancer cell line (A549)Concentration:0-15 μM Incubation Time:72 hours Result:Resulted in a decrease in cell viability from 10 μM to 15 Μm by combining with cisplatin.
  • 体内实验
    Vecuronium bromide (Intravenous injection, 0-5 μM, every 30 min, 2 hours) attenuates the response of carotid sinus nerve activity (CSNA) to hypoxia in a dose-dependent manner and inhibits the neural response of the carotid body to acetylcholine (ACh) in Wister rats. Animal Model:Wister rats weighing 250-350 gDosage:0-5 μM Administration:Intravenous injection; every 30 min; 2 hours Result:Significantly diminished CSNA response to hypoxia at the concentration of 5 μM and reduced carotid sinus nerve response to ACh at 0.5 μM.
  • 同义词
    NC 45
  • 通路
    Endocrinology/Hormones
  • 靶点
    AChR
  • 受体
    nAChR
  • 研究领域
    Neurological Disease
  • 适应症
    ——

化学信息

  • CAS Number
    50700-72-6
  • 分子量
    637.73
  • 分子式
    C34H57BrN2O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    Ethanol: 100 mg/mL (156.8 mM); Water: 4 mg/mL (6.27 mM); DMSO: 100 mg/mL (156.8 mM)
  • SMILES
    CC(O[C@@H]1[C@@H](N2CCCCC2)C[C@]3(C)[C@@]4([H])CC[C@]5(C)[C@H](OC(C)=O)[C@@H]([N+]6(C)CCCCC6)C[C@@]5([H])[C@]4([H])CC[C@@]3([H])C1)=O.[Br-]
  • 化学全称
    1-((2S,3S,5S,8R,9S,10S,13S,14S,16S,17S)-3,17-diacetoxy-10,13-dimethyl-2-(piperidin-1-yl)hexadecahydro-1H-cyclopenta[a]phenanthren-16-yl)-1-methylpiperidin-1-ium bromide

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.Jonsson Fagerlund M, et al. Anesthesiology. 2009 Jun;110(6):1244-52.
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