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880345P

Avanti

PChcPC

Avanti Research™ - A Croda Brand 880345P, powder

Sinônimo(s):

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

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25 MG
R$ 907,00

R$ 907,00

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R$ 907,00

About This Item

Fórmula empírica (Notação de Hill):
C52H94NO9P
Número CAS:
1085528-78-4
Peso molecular:
908.28
Código UNSPSC:
51191904
NACRES:
NA.25

R$ 907,00

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Formulário

powder

embalagem

pkg of 1 × 25 mg (880345P-25mg)

fabricante/nome comercial

Avanti Research™ - A Croda Brand 880345P

tipo de lipídio

cardiolipins
phospholipids

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

O=P([O-])(OCC[N+](C)(C)C)OC[C@H](OC(OC1CC[C@]2(C)C(C1)=CCC3C2CC[C@]4(C)C3CC[C@H]4[C@@H](C)CCCC(C)C)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C52H94NO9P/c1-10-11-12-13-14-15-16-17-18-19-20-21-22-26-49(54)58-38-44(39-60-63(56,57)59-36-35-53(7,8)9)62-50(55)61-43-31-33-51(5)42(37-43)27-28-45-47-30-29-46(41(4)25-23-24-40(2)3)52(47,6)34-32-48(45)51/h27,40-41,43-48H,10-26,28-39H2,1-9H3/t41-,43?,44

chave InChI

KKNCLZSXBLVOBE-JGQOPVPKSA-N

Ações bioquímicas/fisiológicas

PChcPC is a sterol modified phospholipid (SML) known to maintain the stability of bilayers. They do not freely interchange as cholesterol does between the membranes. This new class of phospholipids provides a new tool for biophysical studies on membrane. This may enhance the process of drug delivery mediated by liposome. Especially in organs, prior to the removal of free cholesterol from bilayers of blood, skin or lung.[1]

Embalagem

5 mL Amber Glass Screw Cap Vial (880345P-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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Certificados de análise (COA)

Lot/Batch Number

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F Foglia et al.
Langmuir : the ACS journal of surfaces and colloids, 27(13), 8275-8281 (2011-06-04)
Langmuir isotherm, neutron reflectivity, and small angle neutron scattering studies have been conducted to characterize the monolayers and vesicular bilayers formed by a novel chimeric phospholipid, ChemPPC, that incorporates a cholesteryl moeity and a C-16 aliphatic chain, each covalently linked
Zhaohua Huang et al.
Angewandte Chemie (International ed. in English), 48(23), 4146-4149 (2009-05-09)
Extreme makeover of cholesterol: Cholesterol exchange is a major reason for the instability of liposomes in blood. The formation of a covalent hybrid between cholesterol and glycerophosphocholine preserves the bilayer-stabilizing effect of free cholesterol but prevents its transfer from the
Maryam Iman et al.
International journal of pharmaceutics, 408(1-2), 163-172 (2011-02-01)
1,2-Di-stigma-steryl-hemi-succinoyl-sn-glycero-3-phosphocholine (DSHemsPC) is a new lipid in which two molecules of stigmasterol (an inexpensive plant sterol) are covalently linked via a succinic acid to glycerophosphocholine. Since amphotericin B (AmB) interacts with sterols, we postulated that DSHemsPC could be used in
Zhaohua Huang et al.
Journal of the American Chemical Society, 130(46), 15702-15712 (2008-10-28)
We synthesized a family of sterol-modified glycerophospholipids (SML) in which the sn-1 or sn-2 position is covalently attached to cholesterol and the alternative position contains an aliphatic chain. The SML were used to explore how anchoring cholesterol to a phospholipid

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