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IP7e

CAS No. 500164-74-9

IP7e ( IP 7e | IP-7e | isoxazolo-pyridinone 7e )

产品货号. M27887 CAS No. 500164-74-9

IP7e 是一种 Nurr1 激活剂,EC50 值为 3.9 nM。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥3208 有现货
10MG ¥4771 有现货
25MG ¥7655 有现货
50MG ¥10368 有现货
100MG ¥14013 有现货
500MG ¥28026 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    IP7e
  • 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
    IP7e 是一种 Nurr1 激活剂,EC50 值为 3.9 nM。
  • 产品描述
    IP7e is a Nurr1 activator with an EC50 value of 3.9 nM.(In Vivo):IP7e(10 mg/kg) attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process. IP7e preventive treatment reduces the incidence and the severity of an MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE).
  • 体外实验
    ——
  • 体内实验
    IP7e (Isoxazolo-pyridinone 7e; 10 mg/kg; oral gavage; twice a day) preventive treatment reduces the incidence and the severity of a MS murine model, i.e. experimental autoimmune encephalomyelitis (EAE). IP7e attenuates inflammation and neurodegeneration in spinal cords of EAE mice by an NF-kB pathway-dependent process. Animal Model:Female C57BL/6J mice (6-8 week-old) with experimental autoimmune encephalomyelitis (EAE).Dosage:10 mg/kgAdministration:Oral gavage; twice a day; preventive administration (before the disease onset) from 7 to 23 d.p.i. and therapeutic (after the disease onset) from 21 to 36 d.p.i. Result:Preventive administration delayed the onset and reduces the incidence and severity of EAE, and decreased neuroinflammatory and histopathological alterations in the spinal cord of treated EAE mice. On the contrary, the course of EAE was not influenced by the therapeutic administration.
  • 同义词
    IP 7e | IP-7e | isoxazolo-pyridinone 7e
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    ACMSD
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    500164-74-9
  • 分子量
    390.439
  • 分子式
    C23H22N2O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    In Vitro:?DMSO : 100 mg/mL (256.13 mM)
  • SMILES
    COCCOCc1ccc(cc1)-c1cc2onc(-c3ccccc3)c2c(=O)n1C
  • 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.Pellicciari R, et al. α-Amino-β-carboxymuconate-ε-semialdehyde Decarboxylase (ACMSD) Inhibitors as Novel Modulators of De Novo Nicotinamide Adenine Dinucleotide (NAD+) Biosynthesis. J Med Chem. 2018 Feb 8;61(3):745-759.
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