890703P
Avanti
18:0 EPC (Cl Salt)
Avanti Research™ - A Croda Brand 890703P, powder
Sinônimo(s):
1,2-distearoyl-sn-glycero-3-ethylphosphocholine (chloride salt)
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About This Item
Fórmula empírica (Notação de Hill):
C46H93NO8PCl
Número CAS:
Peso molecular:
854.66
Código UNSPSC:
12352211
NACRES:
NA.25
Produtos recomendados
forma
powder
embalagem
pkg of 1 × 25 mg (890703P-25mg)
fabricante/nome comercial
Avanti Research™ - A Croda Brand 890703P
tipo de lipídio
transfection
cationic lipids
Condições de expedição
dry ice
temperatura de armazenamento
−20°C
cadeia de caracteres SMILES
O=P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O)OCC.[Cl-]
Aplicação
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
Ações bioquímicas/fisiológicas
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.
Embalagem
5 mL Amber Glass Screw Cap Vial (890703P-25mg)
Informações legais
Avanti Research is a trademark of Avanti Polar Lipids, LLC
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
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Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.
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
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)
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
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
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
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