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Key Documents

810282P

Avanti

TopFluor™ PE

Avanti Research™ - A Croda Brand 810282P, powder

Synonym(s):

1-palmitoyl-2-(dipyrrometheneboron difluoride)undecanoyl-sn-glycero-3-phosphoethanolamine

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About This Item

Empirical Formula (Hill Notation):
C45H77BF2N3O8P
CAS Number:
1246355-64-5
Molecular Weight:
867.89
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 mg (810282P-1mg)
pkg of 5 × 1 mg (810282P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 810282P

shipped in

dry ice

storage temp.

−20°C

General description

Phosphoethanolamine (PHOS) is a precursor to phosphatidylcholine and phosphatidylethanolamine. The phosphatidylethanolamine (PE) is a zwitterionic phospholipid.

Biochem/physiol Actions

Phosphatidylethanolamine controls membrane fluidity in eukaryotic cells. Phosphoethanolamine (PHOS) has the ability to repress tumour growth both in vitro and in vivo.

Packaging

5 mL Amber Glass Screw Cap Vial (810282P-1mg)
5 mL Amber Glass Screw Cap Vial (810282P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC
TopFluor is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Phosphoethanolamine and the danger of unproven drugs
Ponde N, et al.
Ecancermedicalscience (2016)
Phosphatidylethanolamine is a key regulator of membrane fluidity in eukaryotic cells
Dawaliby R, et al.
Test, 3658-3667 (2016)
Lipid-protein interactions in membranes
Marsh D
The Membranes of Cells (1990)
Lipid-protein interactions in membranes
Febs Letters, 268(2), 371-375 (1990)
Pei Qiao et al.
Biochemistry, 59(22), 2089-2099 (2020-05-07)
Activation of G-protein-gated inwardly rectifying potassium channels (Kir3.x) requires the direct binding of phosphorylated phosphatidylinositides (PIPs). Previous studies have established that PIP isoforms activate Kir channels to varying degrees and the binding affinity between PIPs and Kir3.2 appears to be
View All Related Papers

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