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Tempol

CAS No. 2226-96-2

Tempol ( 4-hydroxy TEMPO )

产品货号. M13561 CAS No. 2226-96-2

Tempol 是一种超氧化物清除剂,具有神经保护、抗炎和镇痛作用。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
500MG ¥235 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Tempol
  • 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
    Tempol 是一种超氧化物清除剂,具有神经保护、抗炎和镇痛作用。
  • 产品描述
    Tempol is a superoxide scavenger that displays neuroprotective, anti-inflammatory and analgesic effects.(In Vitro):Tempol significantly attenuates H2O2-mediated decrease in mitochondrial respiration and increase in LDH release from rat PT cells, indicating a reduction in cell injury and death. The beneficial actions of Tempol are similar to those obtained using the Fe2+ chelator DEF. However, coadministration of DEF and Tempol does not produce any additional beneficial actions against renal ischemia/reperfusion injury or against oxidative stress-mediated PT cell injury/death. (In Vivo):SOD-mimetic Tempol is able to mimic resveratrol’s effects on heart function. Tempol is administered daily by gavage. Mice treated with Met or Tmp had decreased PR and QTc intervals and increased heart rates compared to peroral vehicle (VEH). These results are similar to that obtained by treatment with RSV. Pre- and post-treatment profiles of individual mice are illustrated. Tempol, a membrane-permeable radical scavenger, reduces oxidant stress-mediated renal dysfunction and injury in the rat. Tempol significantly reduces the increase in urea, creatinine, γGT, AST, NAG, and FENa produced by renal ischemia/reperfusion, suggesting an improvement in both renal function and injury. Tempol also significantly reduces kidney MPO activity and MDA levels, indicating a reduction in PMN infiltration and lipid peroxidation, respectively. Tempol reduces the histologic evidence of renal damage associated with ischemia/reperfusion and caused a substantial reduction in the staining for nitrotyrosine and PARS, suggesting reduced nitrosative and oxidative stress.
  • 体外实验
    Tempol significantly attenuates H2O2-mediated decrease in mitochondrial respiration and increase in LDH release from rat PT cells, indicating a reduction in cell injury and death. The beneficial actions of Tempol are similar to those obtained using the Fe2+ chelator DEF. However, coadministration of DEF and Tempol does not produce any additional beneficial actions against renal ischemia/reperfusion injury or against oxidative stress-mediated PT cell injury/death.
  • 体内实验
    SOD-mimetic Tempol is able to mimic resveratrol’s effects on heart function. Tempol is administered daily by gavage. Mice treated with Met or Tmp had decreased PR and QTc intervals and increased heart rates compared to peroral vehicle (VEH). These results are similar to that obtained by treatment with RSV. Pre- and post-treatment profiles of individual mice are illustrated. Tempol, a membrane-permeable radical scavenger, reduces oxidant stress-mediated renal dysfunction and injury in the rat. Tempol significantly reduces the increase in urea, creatinine, γGT, AST, NAG, and FENa produced by renal ischemia/reperfusion, suggesting an improvement in both renal function and injury. Tempol also significantly reduces kidney MPO activity and MDA levels, indicating a reduction in PMN infiltration and lipid peroxidation, respectively. Tempol reduces the histologic evidence of renal damage associated with ischemia/reperfusion and caused a substantial reduction in the staining for nitrotyrosine and PARS, suggesting reduced nitrosative and oxidative stress.
  • 同义词
    4-hydroxy TEMPO
  • 通路
    Immunology/Inflammation
  • 靶点
    ROS
  • 受体
    ROS
  • 研究领域
    Cancer
  • 适应症
    ——

化学信息

  • CAS Number
    2226-96-2
  • 分子量
    172.24
  • 分子式
    C9H18NO2
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:34 mg/mL (197.39 mM); Ethanol:34 mg/mL (197.39 mM); Water:34 mg/mL (197.39 mM)
  • SMILES
    [O]N1C(C)(C)CC(O)CC1(C)C
  • 化学全称
    1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl-

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. Mitchell JB, et al. Arch Biochem Biophys, 1991, 289(1), 62-70.
产品手册
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