• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

SEA-0400

CAS No. 223104-29-8

SEA-0400 ( SEA0400 | SEA-0400 | SEA 0400 )

产品货号. M17444 CAS No. 223104-29-8

SEA0400 是 Na+/Ca2+ 交换剂的选择性抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥373 有现货
5MG ¥599 有现货
10MG ¥1077 有现货
25MG ¥1968 有现货
50MG ¥3216 有现货
100MG ¥4836 有现货
500MG ¥10692 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    SEA-0400
  • 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
    SEA0400 是 Na+/Ca2+ 交换剂的选择性抑制剂。
  • 产品描述
    SEA0400 is a Na+/Ca2+ exchanger 1 inhibitor. SEA0400 prevents dopaminergic neurotoxicity in an MPTP mouse model of Parkinson's disease. SEA0400 reduces calcium overload induced by ischemia and reperfusion in mouse ventricular myocytes. SEA0400 attenuates sodium nitroprusside-induced apoptosis in cultured rat microglia. SEA0400, preserves cardiac function and high-energy phosphates against ischemia/reperfusion injury.
  • 体外实验
    SEA0400 inhibits Na+-dependent 45Ca2+ uptake in cultured neurons, astrocytes, and microglia. IC50 values of SEA0400 are 33 nM (neurons), 5.0 nM (astrocytes), and 8.3 nM (microglia). SEA0400 prevents sodium nitroprusside (SNP) to increase ERK and p38 MAPK phosphorylation, and production of reactive oxygen species (ROS) in an extracellular Ca2+-dependent manner.
  • 体内实验
    SEA0400 (3 mg/kg + 3 mg/kg/h for 2 h, i.v.) attenuates the infarct volume in the cerebral cortex and striatum, does not affect the mean the regional cortical blood flow in anesthetized rats. SEA0400 protects against the dopaminergic neurotoxicity (determined by dopamine levels in the midbrain and striatum, tyrosine hydroxylase immunoreactivity in the substantia nigra and striatum, striatal dopamine release, and motor deficits) in MPTP-treated C57BL/6J mice.
  • 同义词
    SEA0400 | SEA-0400 | SEA 0400
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    NCX
  • 研究领域
    Cardiovascular Disease
  • 适应症
    ——

化学信息

  • CAS Number
    223104-29-8
  • 分子量
    371.38
  • 分子式
    C21H19F2NO3
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 32 mg/mL; 86.17 mM
  • SMILES
    CCOc1cc(c(cc1)Oc1ccc(cc1)OCc1c(ccc(c1)F)F)N
  • 化学全称
    2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline

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. Matsuda, T., et al. J.Pharmacol.Exp.Ther. 2001, 298(1), 249-256.
产品手册
关联产品
  • Asperuloside

    Asperuloside 是一种环烯醚萜,来源于蛇舌草,具有抗炎活性。Asperuloside 可抑制诱导型一氧化氮合酶 (iNOS),抑制 NF-κB 和 MAPK 信号通路。

  • KYP-2047

    KYP-2047 是一种非常有效的选择性脯氨酰寡肽酶 (POP) 抑制剂。在细胞系中,氧化应激诱导 α-突触核蛋白的强烈聚集,低浓度的 KYP-2047 显着减少了具有 α-突触核蛋白包涵体的细胞数量,而废除 α-突触核蛋白和 PREP 的共定位。

  • Propiosyringone

    丙丁香酮来自蓝桉木被木材腐烂真菌降解。