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144371-68-6

144371-68-6 Structure

144371-68-6 Structure
IdentificationBack Directory
[Name]

1-(1Z-octadecenyl)-2-oleoyl-sn-glycero-3-phosphoethanolaMine
[CAS]

144371-68-6
[Synonyms]

C18(Plasm)-18:1 PE
1-(1Z-octadecenyl)-2-oleoyl-sn-glycero-3-phosphoethanolaMine
1-(1Z-OCTADECENYL)-2-OLEOYL-SN-GLYCERO-3-PHOSPHOETHANOLAMINE;C18(PLASM)-18:1 PE
[Molecular Formula]

C41H80NO7P
[MDL Number]

MFCD22416571
[MOL File]

144371-68-6.mol
[Molecular Weight]

730.05
Chemical PropertiesBack Directory
[Boiling point ]

750.5±70.0 °C(Predicted)
[density ]

0.985±0.06 g/cm3(Predicted)
[storage temp. ]

-20°C
[form ]

powder
[pka]

1.18±0.50(Predicted)
Hazard InformationBack Directory
[Uses]

C18(Plasm)-18:1 PE has been used for lipid purification and fatty acid extraction. It has also been used for lipopolysaccharide (LPS)-mediated beta rich prion protein PrPβ conversion.
[Definition]

ChEBI: 1-(1Z-octadecenyl)-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine is a 1-(alk-1-enyl)-2-acyl-sn-glycero-3-phosphoethanolamine in which the alk-1-enyl and acyl groups are specified as (1Z)-octadecenyl and (9Z)-octadecenoyl respectively. It has a role as a mouse metabolite. It is functionally related to an oleic acid. It is a tautomer of a 1-(1Z-octadecenyl)-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine zwitterion.
[Biological Activity]

Phosphatidylethanolamine forms pure lipid structures. It maintains membrane fluidity in eukaryotic cells. Phosphatidylethanolamine plays a critical role in autophagycell division and protein folding. It acts as a precursor for the synthesis of various protein modifications. Phosphatidylethanolamine functions as an intermediate for the synthesis of glycerophospholipid classes.
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