ChemicalBook--->CAS DataBase List--->883288-78-6

883288-78-6

883288-78-6 Structure

883288-78-6 Structure
IdentificationBack Directory
[Name]

Phosphoric acid, mono(2-aminoethyl) mono(2,3-dihydroxypropyl) ester, monosodium salt (9CI)
[CAS]

883288-78-6
[Synonyms]

LUM88786
Phosphoric acid, mono(2-aminoethyl) mono(2,3-dihydroxypropyl) ester, monosodium salt (9CI)
[Molecular Formula]

C5H15NNaO6P
[MOL File]

883288-78-6.mol
[Molecular Weight]

239.14
Chemical PropertiesBack Directory
[storage temp. ]

-20°C
[solubility ]

Water: slightly soluble
[form ]

A solid
[Water Solubility ]

Water: slightly soluble
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H332-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P330-P302+P352-P321-P304+P340-P305+P351+P338-P332+P313-P362+P364-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Glycerophosphorylethanolamine (GroPEtn) sodium is an active phosphodiester metabolite of Phosphatidylethanolamine (HY-W250118). Glycerophosphorylethanolamine sodium promotes the aggregation of amyloid β-protein (Aβ (1-40)) in vitro. Glycerophosphorylethanolamine sodium can be used in the field of neurodegenerative diseases, such as Alzheimer’s disease research[1].
[Biological Activity]

Glycerophosphorylethanolamine is an active phosphodiester metabolite of phosphatidylethanolamine.1,2 It promotes aggregation of amyloid-β (1-40) (Aβ40) in vitro, and levels of glycerophosphorylethanolamine are elevated in postmortem brains isolated from patients with Alzheimer’s disease.
[References]

1.Klunk, W.E., Xu, C.J., McClure, R.J., et al.Aggregation of β-amyloid peptide is promoted by membrane phospholipid metabolites elevated in Alzheimer’s disease brainJ. Neurochem.69(1)266-272(1997) 2.Blusztajn, J.K., Lopez Gonzalez-Coviella, I., Logue, M., et al.Levels of phospholipid catabolic intermediates, glycerophosphocholine and glycerophosphoethanolamine, are elevated in brains of Alzheimer’s disease but not of Down’s syndrome patientsBrain Res.536(1-2)240-244(1990)
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