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Sodium Tetradecyl Sulfate

CAS No. 1191-50-0

Sodium Tetradecyl Sulfate ( Tetradecyl sodiuM sulfate )

产品货号. M28806 CAS No. 1191-50-0

Sodium Tetradecyl Sulfate 是一种具有抗血栓作用的清洁硬化剂,常用于治疗静脉曲张。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
25MG ¥332 有现货
50MG ¥462 有现货
100MG ¥664 有现货
200MG ¥980 有现货
500MG 获取报价 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Sodium Tetradecyl Sulfate
  • 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
    Sodium Tetradecyl Sulfate 是一种具有抗血栓作用的清洁硬化剂,常用于治疗静脉曲张。
  • 产品描述
    Sodium Tetradecyl Sulfate is a detergent sclerosant with antithrombotic effects and commonly used for the treatment of varicose veins.(In Vitro):Proteins C, S and antithrombin (AT) were assayed in normal plasma treated with increasing concentrations of Sodium Tetradecyl Sulfate. High concentration (>0.6%) Sodium Tetradecyl Sulfate significantly destroyed proteins C, S and AT. Sodium Tetradecyl Sulfate potentiated the anticoagulant effect of APC. Sodium Tetradecyl Sulfate mimicked AT and demonstrated significant anti-Xa and anti-IIa activity. STS demonstrated a weak anticoagulant profile to heparin. It also significantly potentiated the anticoagulant effect of heparin.(In Vivo):i.v. + p.v. injection of Sodium Tetradecyl Sulfate and hydroxy polyethoxy dodecan provided a high degree of efficacy as regards vein occlusion. On the other hand, i.v. + p.v. injection induced a severe inflammation and necrosis of the tissues surrounding the sclerosed vein.
  • 体外实验
    ——
  • 体内实验
    ——
  • 同义词
    Tetradecyl sodiuM sulfate
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    NMDA
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1191-50-0
  • 分子量
    316.43
  • 分子式
    C14H29NaO4S
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (316.03 mM)
  • SMILES
    [Na+].CCCCCCCCCCCCCCOS([O-])(=O)=O
  • 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.Walters MR, et al. Early clinical experience with the novel NMDA receptor antagonist CNS 516Br J Clin Pharmacol. 2002 Mar;53(3):305-11.
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