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Dokumente

P4142

Sigma-Aldrich

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

≥98% (GC), ≥99% (TLC)

Synonym(e):

1-(cis-9-Octadecenoyl)-2-hexadecanoyl-sn-glycero-3-phosphocholine, L-α-Phosphatidylcholine, β-palmitoyl-γ-oleoyl

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About This Item

Empirische Formel (Hill-System):
C42H82NO8P
CAS-Nummer:
59491-62-2
Molekulargewicht:
760.08
MDL-Nummer:
MFCD00063534
UNSPSC-Code:
12352211
PubChem Substanz-ID:
24898505
NACRES:
NA.25

Biologische Quelle

synthetic (organic)

Assay

≥98% (GC)
≥99% (TLC)

Form

powder

Funktionelle Gruppe

phospholipid

Lipid-Typ

phosphoglycerides

Versandbedingung

ambient

Lagertemp.

−20°C

SMILES String

CCCCCCCCCCCCCCCC(=O)O[C@@H](COC(=O)CCCCCCC\C=C/CCCCCCCC)COP(O)(=O)OCC[N](C)(C)C

InChI

1S/C42H83NO8P/c1-6-8-10-12-14-16-18-20-21-23-24-26-28-30-32-34-41(44)48-38-40(39-50-52(46,47)49-37-36-43(3,4)5)51-42(45)35-33-31-29-27-25-22-19-17-15-13-11-9-7-2/h20-21,40H,6-19,22-39H2,1-5H3,(H,46,47)/b21-20-

InChIKey

ZLPCRCSDGDOSCT-MRCUWXFGSA-N

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Cell biology. Gentle slam.
R Peters et al.
Science (New York, N.Y.), 282(5397), 2213-2214 (1999-01-16)
A M Jiménez-Monreal et al.
Biochemistry, 38(24), 7747-7754 (1999-07-01)
The activation of protein kinase C alpha was studied by using a lipid system consisting of 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC)/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoserine (POPS) (molar ratio 4:1) and different proportions of 1-palmitoyl-2-oleoyl-sn-glycerol (POG). The phase behavior of the lipidic system was characterized by using differential
Federico Karagulian et al.
Physical chemistry chemical physics : PCCP, 10(4), 528-541 (2008-01-10)
The ozonolysis of an approximately one monolayer film of 1-oleoyl-2-palmitoyl-sn-glycero-3-phosphocholine (OPPC) on NaCl was followed in real time using diffuse reflection infrared Fourier transform spectrometry (DRIFTS) at 23 degrees C. Matrix-assisted laser desorption/ionization (MALDI) mass spectrometry and Auger electron spectroscopy
Jeffrey F Ellena et al.
Journal of medicinal chemistry, 45(25), 5534-5542 (2002-12-03)
There is considerable interest in the use of perfluorocarbons as oxygen carriers in clinical settings; however, little is known regarding the molecular interactions made by these apolar compounds with biological membranes or their effect on membrane structure. NMR spectroscopy was
Mojtaba Bagheri et al.
Antimicrobial agents and chemotherapy, 53(3), 1132-1141 (2008-12-24)
Early studies of immobilized peptides mainly focused upon the relationship between structural properties and the activity of soluble and surface-tethered sequences. The intention of this study was to analyze the influence of immobilization parameters upon the activity profile of peptides.
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