中文名 | SEA0400 |
英文名 | SEA0400 |
别名 | SEA0400游离态 NA+-CA2+EXCHANGER抑制剂(SEA0400) 2-[4-[(2,5-二氟苯基)甲氧基]苯氧基]-5-乙氧基苯胺 |
英文别名 | CS-1043 SEA0400 SEA 0400 SEA-0400 SEA-0400 2-(4-((2,5-DIFLUOROBENZYL)OXY)PHENOXY)-5-ETHOXYANILINE 2-[4-[(2,5-difluorophenyl)methoxy]phenoxy]-5-ethoxyaniline 2-[4-[(2,5-Difluorophenyl)methoxy]phenoxy]-5-ethoxybenzenamine BenzenaMine, 2-[4-[(2,5-difluorophenyl)Methoxy]phenoxy]-5-ethoxy- |
CAS | 223104-29-8 |
化学式 | C21H19F2NO3 |
分子量 | 371.38 |
存储条件 | Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
体外研究 | SEA0400 inhibits Na + -dependent 45 Ca 2+ uptake in cultured neurons, astrocytes, and microglia. IC 50 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 Ca 2+ -dependent manner. |
体内研究 | 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. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.693 ml | 13.463 ml | 26.927 ml |
5 mM | 0.539 ml | 2.693 ml | 5.385 ml |
10 mM | 0.269 ml | 1.346 ml | 2.693 ml |
5 mM | 0.054 ml | 0.269 ml | 0.539 ml |
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