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S81987

TM5275 (sodium)

MedMol 96%
  • 英文名:
  • TM5275 (sodium)
  • 别名:
  • TM5275; sodium 2-(2-(2-(4-benzhydrylpiperazin-1-yl)-2-oxoethoxy)acetamido)-5-chlorobenzoate;
  • CAS号:
  • 1103926-82-4
  • 分子式:
  • C28H28ClN3NaO5+
  • 分子量:
  • 544.9813
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
MedMol S81987-1mg 96% ¥251.60元 10 - - - EA 加入购物车
MedMol S81987-2mg 96% ¥448.80元 10 - - - EA 加入购物车
MedMol S81987-5mg 96% ¥630.00元 10 - - - EA 加入购物车
MedMol S81987-10mg 96% ¥952.00元 7 - - - EA 加入购物车
MedMol S81987-25mg 96% ¥1564.00元 2 - - - EA 加入购物车
源叶(MedMol) S81987-50mg 96% ¥2720.00元 预计交期:2-3天 - - - EA 加入购物车
源叶(MedMol) S81987-100mg 96% ¥4896.00元 预计交期:2-3天 - - - EA 加入购物车
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  • 产品描述: TM5275 sodium is a plasminogen activator inhibitor (PAI-1) with an IC50 of 6.95 μM.
  • 靶点: IC50: 6.95 μM (PAI-1);PAI-1
  • 体外研究:
    Docking studies shows that TM5275 binds to strand 4 of the A β-sheet (s4A) position of PAI-1. TM5275 is a selective PAI-1 and (up to 100 μM) does not interfere with other serpin/serine protease systems. TM5275 at concentrations of 20 and 100 μM significantly prolongs the retention of tPA-GFP on VECs by inhibiting tPA-GFP-PAI-1 high-molecular-weight complex formation. TM5275 enhances the time-dependent accumulation of plasminogen as well as the dissolution of fibrin clots on and around the tPA-GFP-expressing cells. Cell viability at 72 h treatment is decreased with 70-100 μM TM5275 in ES-2 and JHOC-9 cells. From 48 h up to 96 h, cell growth is suppressed with 100 μM TM5275. Active PAI-1 in cell culture media is significantly decreased in cells treated with 100 μM TM5275 compared to control treatment. TM5275 is suggested to exert anti-proliferative effects in ovarian cancer with high PAI-1 expression
  • 体内研究:
    TM5275 exhibits a favorable pharmacokinetics profile and very low toxicity to mice and rats. In rat thrombosis models. Blood clot weights are significantly lower in rats administered 10 and 50 mg/kg of TM5275 (60.9±3.0 and 56.8±2.8 mg, respectively) than in vehicle-treated rats (72.5±2.0 mg). The antithrombotic effectiveness of TM5275 (50 mg/kg) is equivalent to that of ticlopidine (500 mg/kg), a reference antithrombotic compound. Plasma concentration of TM5275 reaches 17.5±5.2 μM after a dose of 10 mg/kg. TM5275 (5 mg/kg) combined with tPA (0.3 mg/kg) significantly enhances the antithrombotic effect of tPA (0.3 mg/kg) alone and provides a benefit similar to that of a high tPA dose (3 mg/kg)
  • 参考文献:
    1. Izuhara Y, et al. A novel inhibitor of plasminogen activator inhibitor-1 provides antithrombotic benefits devoid of bleeding effect in nonhuman primates. J Cereb Blood Flow Metab. 2010 May;30(5):904-12. 2. Yasui H, et al. TM5275 prolongs secreted tissue plasminogen activator retention and enhances fibrinolysis on vascular endothelial cells. Thromb Res. 2013 Jul;132(1):100-5. 3. Mashiko S, et al. Inhibition of plasminogen activator inhibitor-1 is a potential therapeutic strategy in ovarian cancer. Cancer Biol Ther. 2015;16(2):253-60.
  • 溶解性: soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 1.835 ml 9.175 ml 18.349 ml
    5 mM 0.367 ml 1.835 ml 3.67 ml
    10 mM 0.183 ml 0.917 ml 1.835 ml
    50 mM 0.037 ml 0.183 ml 0.367 ml
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