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01991

Sigma-Aldrich

2-Oleoyl-1-palmitoyl-sn-glycero-3-phosphoethanolamin

≥95% (TLC)

Synonym(e):

1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamin, 3-sn-Phosphatidylethanolamin, 2-Oleoyl-1-palmitoyl, L-β-Oleoyl-γ-palmitoyl-α-cephalin, POPE

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About This Item

Lineare Formel:
C39H76NO8P
CAS-Nummer:
26662-94-2
Molekulargewicht:
718.00
EG-Nummer:
247-894-0
MDL-Nummer:
MFCD00042829
UNSPSC-Code:
51191904
PubChem Substanz-ID:
329747382
NACRES:
NA.85

Qualitätsniveau

100

Assay

≥95% (TLC)

Form

solid

Funktionelle Gruppe

amine

Lipid-Typ

phosphoglycerides

Lagertemp.

−20°C

SMILES String

CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCCN)OC(=O)CCCCCCC\C=C\CCCCCCCC

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+

InChIKey

FHQVHHIBKUMWTI-ISLYRVAYSA-N

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Verwandte Kategorien

Biochem./physiol. Wirkung

Lipid effects on the topography of membrane-associated hydrophobic helices, membrane targeting by the GRP1 PH domain.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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16:0-18:1 PG Avanti Research™ - A Croda Brand

Avanti

840457P

16:0-18:1 PG

16:0–18:1 PS (POPS) Avanti Research™ - A Croda Brand

Avanti

840034P

16:0–18:1 PS (POPS)

Ju He et al.
Journal of lipid research, 49(8), 1807-1815 (2008-05-13)
The general receptor for phosphoinositides isoform 1 (GRP1) is recruited to the plasma membrane in response to activation of phosphoinositide 3-kinases and accumulation of phosphatidylinositol 3,4,5-trisphosphate [PtdIns(3,4,5)P(3)]. GRP1's pleckstrin homology (PH) domain recognizes PtdIns(3,4,5)P(3) with high specificity and affinity, however
R Willumeit et al.
Journal of materials science. Materials in medicine, 18(2), 367-380 (2007-02-27)
Bio-interfaces such as bio-membranes are of outmost importance for a variety of live processes. Among them are cell-interactions which take place in, on or through cell membranes. Therefore we propose to cover metallic surfaces with phospholipids to facilitate cell-material interaction.
Khurshida Shahidullah et al.
Journal of molecular biology, 379(4), 704-718 (2008-05-16)
To investigate the effect of lipid structure upon the membrane topography of hydrophobic helices, the behavior of hydrophobic peptides was studied in model membrane vesicles. To define topography, fluorescence and fluorescence quenching methods were used to determine the location of
Hui-Hsu Gavin Tsai et al.
Biochimica et biophysica acta, 1838(6), 1529-1535 (2014-01-29)
Membrane fusion is essential for intracellular trafficking and virus infection, but the molecular mechanisms underlying the fusion process remain poorly understood. In this study, we employed all-atom molecular dynamics simulations to investigate the membrane fusion mechanism using vesicle models which
Y Murakami et al.
Cell death and differentiation, 21(11), 1746-1757 (2014-07-19)
The CD300 receptor family members are a group of molecules that modulate a variety of immune cell processes. We show that mouse CD300b (CLM7/LMIR5), expressed on myeloid cells, recognizes outer membrane-exposed phosphatidylserine (PS) and does not, as previously reported, directly
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