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Ximelagatran

CAS No. 192939-46-1

Ximelagatran ( H 376-95 | H 376/95 | H 37695 | H-37695 | H37695 | EXANTA )

产品货号. M26866 CAS No. 192939-46-1

希美加群是一种直接凝血酶抑制剂,可以口服,仅通过抑制凝血酶的作用来发挥作用。希美加群在体内转化为活性剂美拉加群。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1004 有现货
10MG ¥1750 有现货
25MG ¥4026 有现货
50MG ¥4528 有现货
100MG ¥6456 有现货
200MG ¥9072 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
    Ximelagatran
  • 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
    希美加群是一种直接凝血酶抑制剂,可以口服,仅通过抑制凝血酶的作用来发挥作用。希美加群在体内转化为活性剂美拉加群。
  • 产品描述
    Ximelagatran, a direct thrombin inhibitor, can be taken orally and acts solely by inhibiting the actions of thrombin. Ximelagatran is converted to the active agent melagatran in vivo.(In Vitro):Ximelagatran is an orally administered direct thrombin inhibitor under development as an anticoagulant agent for prophylaxis against and treatment of thromboembolism. Ximelagatran is rapidly absorbed and quickly converted into its active form Melagatran, a reversible, active-site inhibitor of both free and clot-bound thrombin that has stable and reproducible pharmacokinetic properties. Initial studies have shown Ximelagatran to have good efficacy and safety in the prevention of venous thromboembolism after total knee or total hip replacement.
  • 体外实验
    Ximelagatran is an orally administered direct thrombin inhibitor under development as an anticoagulant agent for prophylaxis against and treatment of thromboembolism. Ximelagatran is rapidly absorbed and quickly converted into its active form Melagatran, a reversible, active-site inhibitor of both free and clot-bound thrombin that has stable and reproducible pharmacokinetic properties. Initial studies have shown Ximelagatran to have good efficacy and safety in the prevention of venous thromboembolism after total knee or total hip replacement.
  • 体内实验
    ——
  • 同义词
    H 376-95 | H 376/95 | H 37695 | H-37695 | H37695 | EXANTA
  • 通路
    Autophagy
  • 靶点
    Thrombin
  • 受体
    H1 receptor| HCV
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    192939-46-1
  • 分子量
    473.574
  • 分子式
    C24H35N5O5
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 250 mg/mL (527.91 mM)
  • SMILES
    CCOC(=O)CN[C@H](C1CCCCC1)C(=O)N1CC[C@H]1C(=O)NCc1ccc(\C=N\NO)cc1
  • 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.Enright BP, et al. Effects of the histamine H1 antagonist Chlorcyclizine on rat fetal palate development. Birth Defects Res B Dev Reprod Toxicol. 2010 Dec;89(6):474-84.
产品手册
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