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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)
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规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥373 | 有现货 |
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5MG | ¥599 | 有现货 |
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10MG | ¥1077 | 有现货 |
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25MG | ¥1968 | 有现货 |
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50MG | ¥3216 | 有现货 |
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100MG | ¥4836 | 有现货 |
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500MG | ¥10692 | 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SEA-0400
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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SEA0400 是 Na+/Ca2+ 交换剂的选择性抑制剂。
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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.
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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.
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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.
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同义词SEA0400 | SEA-0400 | SEA 0400
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通路Others
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靶点Other Targets
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受体NCX
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研究领域Cardiovascular Disease
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适应症——
化学信息
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CAS Number223104-29-8
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分子量371.38
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分子式C21H19F2NO3
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 32 mg/mL; 86.17 mM
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SMILESCCOc1cc(c(cc1)Oc1ccc(cc1)OCc1c(ccc(c1)F)F)N
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化学全称2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline
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. Matsuda, T., et al. J.Pharmacol.Exp.Ther. 2001, 298(1), 249-256.
产品手册
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