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890703P

Avanti

18:0 EPC (Cl Salt)

Avanti Research™ - A Croda Brand 890703P, powder

Synonym(e):

1,2-distearoyl-sn-glycero-3-ethylphosphocholine (chloride salt)

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About This Item

Empirische Formel (Hill-System):
C46H93NO8PCl
CAS-Nummer:
328268-13-9
Molekulargewicht:
854.66
UNSPSC-Code:
12352211
NACRES:
NA.25

Form

powder

Verpackung

pkg of 1 × 25 mg (890703P-25mg)

Hersteller/Markenname

Avanti Research™ - A Croda Brand 890703P

Lipid-Typ

transfection
cationic lipids

Versandbedingung

dry ice

Lagertemp.

−20°C

SMILES String

O=P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O)OCC.[Cl-]

Verwandte Kategorien

Anwendung

1,2-distearoyl-sn-glycero-3-ethylphosphocholine (18:0 EPC) might be used:
  • to study its effect on the synergistic antimicrobial action of eugenol against Escherichia coli C600
  • to test its use in the formation of lipid nanoparticle variants
  • as a constituent of the microbubble formulation
  • to prepare lipid monolayer for the study on the nature and orientation of interaction between graphene oxide (GO) and lipid models

Biochem./physiol. Wirkung

Cationic lipids are useful co-adjuvants for promoting the immunogenicity of vaccines. 1,2-distearoyl-sn-glycero-3-ethylphosphocholine (18:0 EPC) is a cationic lipid and is found to upregulate cluster of differentiation (CD)80 and CD86 co-stimulatory molecules. The hydrophilic moiety and the acyl chains of the cationic lipids highly influences their co-stimulatory action.

Verpackung

5 mL Amber Glass Screw Cap Vial (890703P-25mg)

Rechtliche Hinweise

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

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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Die Dokumentenbibliothek aufrufen

Caroline Lonez et al.
Advanced drug delivery reviews, 64(15), 1749-1758 (2012-05-29)
Cationic liposomes are commonly used as a transfection reagent for DNA, RNA or proteins and as a co-adjuvant of antigens for vaccination trials. A high density of positive charges close to cell surface is likely to be recognized as a
Haoshu Zhang et al.
Applied and environmental microbiology, 83(21) (2017-08-27)
In this study, the effect of individual lecithin phospholipids on the antimicrobial properties of eugenol against Escherichia coli C600 was investigated. We tested five major phospholipids common in soy or egg lecithin (1,2-dihexadecanoyl-sn-glycero-3-phosphocholine [DPPC], 1,2-dioctadecanoyl-sn-glycero-3-phosphocholine [DSPC], 1,2-dihexadecanoyl-sn-glycero-3-phosphoethanolamine [DPPE], 1,2-dihexadecanoyl-sn-glycero-3-phosphate [sodium
Head groups of lipids govern the interaction and orientation between graphene oxide and lipids
Li S, et al.
The Journal of Physical Chemistry C, 117(31), 16150-16158 (2013)
Caroline Lonez et al.
Progress in lipid research, 47(5), 340-347 (2008-04-22)
Cationic lipids are positively charged amphiphilic molecules which, for most of them, form positively charged liposomes, sometimes in combination with a neutral helper lipid. Such liposomes are mainly used as efficient DNA, RNA or protein carriers for gene therapy or
Jurriaan J J Gillissen et al.
Langmuir : the ACS journal of surfaces and colloids, 34(1), 503-511 (2017-12-05)
Enclosed lipid bilayer structures, referred to as liposomes or lipid vesicles, have a wide range of biological functions, such as cellular signaling and membrane trafficking. The efficiency of cellular uptake of liposomes, a key step in many of these functions
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