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850757P

Avanti

16:0-18:1 PE

Avanti Polar Lipids

Synonym(s):

1-hexadecanoyl-2-(9Z-octadecenoyl)-sn-glycero-3-phosphoethanolamine; POPE; PE(16:0/18:1(9Z)); 110637

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About This Item

Empirical Formula (Hill Notation):
C39H76NO8P
CAS Number:
26662-94-2
Molecular Weight:
718.00
UNSPSC Code:
51191904
NACRES:
NA.25

description

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine

Assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 1 g (850757P-1g)
pkg of 2 × 100 mg (850757P-200mg)
pkg of 5 × 100 mg (850757P-500mg)
pkg of 1 × 25 mg (850757P-25mg)

manufacturer/tradename

Avanti Polar Lipids

lipid type

cardiolipins
phospholipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C39H76NO8P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-39(42)48-37(36-47-49(43,44)46-34-33-40)35-45-38(41)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,37H,3-16,19-36,40H2,1-2H3,(H,43,44)/b18-17-

InChI key

FHQVHHIBKUMWTI-ZCXUNETKSA-N

Application

16:0-18:1 PE has been used for the preparation of large unilamellar vesicles (LUV). It has also been used for the preparation of liposomes for dual polarisation interferometry (DPI).

Packaging

5 mL Clear Glass Sealed Ampule (850757P-200mg)
5 mL Clear Glass Sealed Ampule (850757P-25mg)
5 mL Clear Glass Sealed Ampule (850757P-500mg)
60 mL Amber Wide Mouth Screw Cap Glass Bottle (850757P-1g)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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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The use of liprotides to stabilize and transport hydrophobic molecules
Pedersen JN, et al.
Biochemistry, 54(31), 4815-4823 (2015)
Using protein-fatty acid complexes to improve vitamin D stability
Pedersen JN, et al.
Journal of Dairy Science, 99(10), 7755-7767 (2016)
Examination of the Interaction between a Membrane Active Peptide and Artificial Bilayers by Dual Polarisation Interferometry
Payne JAE, et al.
Bio-protocol, 7(1), e2087-e2087 (2017)
Tânia Silva et al.
Langmuir : the ACS journal of surfaces and colloids, 34(5), 2158-2170 (2018-01-07)
An understanding of the mechanism of action of antimicrobial peptides is fundamental to the development of new and more active antibiotics. In the present work, we use a wide range of techniques (SANS, SAXD, DSC, ITC, CD, and confocal and
Charles G Cranfield et al.
Langmuir : the ACS journal of surfaces and colloids, 33(26), 6630-6637 (2017-06-14)
Cyclotides are cyclic disulfide-rich peptides that are chemically and thermally stable and possess pharmaceutical and insecticidal properties. The activities reported for cyclotides correlate with their ability to target phosphatidylethanolamine (PE)-phospholipids and disrupt cell membranes. However, the mechanism by which this
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