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Catalog: | HY-15515 |
Brand: | MCE |
CAS: | 223104-29-8 |
MDL | MFCD07772188 |
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Molecular Weight | 371.38 |
Molecular Formula | C21H19F2NO3 |
SMILES | NC1=CC(OCC)=CC=C1OC2=CC=C(OCC3=CC(F)=CC=C3F)C=C2 |
SEA0400 is a novel and selective inhibitor of the Na + -Ca 2+ exchanger ( NCX ), inhibiting Na + -dependent Ca 2+ uptake in cultured neurons, astrocytes, and microglia with IC 50 s of from 5 to 33 nM.
IC50: 5-33 nM (NCX)
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) [1] . 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 [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
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 [1] . 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 [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : ≥ 32 mg/mL ( 86.17 mM )
* "≥" means soluble, but saturation unknown.
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.6927 mL | 13.4633 mL | 26.9266 mL |
5 mM | 0.5385 mL | 2.6927 mL | 5.3853 mL |
10 mM | 0.2693 mL | 1.3463 mL | 2.6927 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 2.5 mg/mL (6.73 mM); Clear solution
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