
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)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1004 | 有现货 |
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10MG | ¥1750 | 有现货 |
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25MG | ¥4026 | 有现货 |
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50MG | ¥4528 | 有现货 |
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100MG | ¥6456 | 有现货 |
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200MG | ¥9072 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Ximelagatran
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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
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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。
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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.
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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.
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体内实验——
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同义词H 376-95 | H 376/95 | H 37695 | H-37695 | H37695 | EXANTA
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通路Autophagy
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靶点Thrombin
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受体H1 receptor| HCV
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研究领域——
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适应症——
化学信息
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CAS Number192939-46-1
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分子量473.574
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分子式C24H35N5O5
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纯度>98% (HPLC)
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溶解度In Vitro:?DMSO : 250 mg/mL (527.91 mM)
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SMILESCCOC(=O)CN[C@H](C1CCCCC1)C(=O)N1CC[C@H]1C(=O)NCc1ccc(\C=N\NO)cc1
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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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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