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223104-29-8

中文名稱 2-[4-[(2,5-二氟苯基)甲氧基]苯氧基]-5-乙氧基苯胺
英文名稱 SEA-0400
CAS 223104-29-8
分子式 C21H19F2NO3
分子量 371.38
MOL 文件 223104-29-8.mol
更新日期 2024/06/17 17:25:40
223104-29-8 結(jié)構(gòu)式 223104-29-8 結(jié)構(gòu)式

基本信息

中文別名
NA+-CA2+EXCHANGER抑制劑(SEA0400)
2-[4-[(2,5-二氟苯基)甲氧基]苯氧基]-5-乙氧基苯胺
英文別名
CS-1043
SEA-0400
SEA 0400
SEA-0400
SEA0400 >=98% (HPLC)
SEA 0400
SEA-0400
SEA0400
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-
所屬類別
生物化工:激動(dòng)劑抑制劑

物理化學(xué)性質(zhì)

沸點(diǎn)485.0±45.0 °C(Predicted)
密度1.254±0.06 g/cm3(Predicted)
儲(chǔ)存條件Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
溶解度insoluble in H2O; ≥18.57 mg/mL in DMSO; ≥46.4 mg/mL in EtOH with ultrasonic
酸度系數(shù)(pKa)4.04±0.10(Predicted)
形態(tài)固體
顏色White to khaki

常見(jiàn)問(wèn)題列表

生物活性
SEA0400 是一種選擇性的 Na+-Ca2+ exchanger (NCX) 的強(qiáng)效抑制劑,可抑制神經(jīng)細(xì)胞、星形膠質(zhì)細(xì)胞和小膠質(zhì)細(xì)胞中Na+依賴性的Ca2+吸收,對(duì)應(yīng)的IC50值分別為33 nM、5.0 nM和8.3 nM。SEA0400 可防止硝普鈉 (SNP) 提高 ERK 和 p38 MAPK 的磷酸化和通過(guò)細(xì)胞外Ca2+依賴的方式增強(qiáng)reactive oxygen species (ROS) 的產(chǎn)生。
靶點(diǎn)
TargetValue
p38 MAPK
()
ERK
()
ROS
()
NCX
(in cultured astrocytes)
5.0 nM
NCX
(in cultured microglia)
8.3 nM
體外研究

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.

體內(nèi)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.

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