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Key Documents

999971P

Avanti

1-C16 Ether MG

Avanti Polar Lipids 999971P, powder

Sinônimo(s):

1-O-hexadecyl-sn-glycerol (HG)

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About This Item

Fórmula empírica (Notação de Hill):
C19H40O3
Número CAS:
Peso molecular:
316.52
Código UNSPSC:
51191904
NACRES:
NA.25

forma

powder

embalagem

pkg of 1 × 250 mg (999971P-250mg)

fabricante/nome comercial

Avanti Polar Lipids 999971P

tipo de lipídio

phospholipids
neutral lipids

Condições de expedição

dry ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

[H][C@@](CO)(O)COCCCCCCCCCCCCCCCC

InChI

1S/C19H40O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-22-18-19(21)17-20/h19-21H,2-18H2,1H3

chave InChI

OOWQBDFWEXAXPB-UHFFFAOYSA-N

Descrição geral

1-C16 Ether MG or 1-O-hexadecyl-sn-glycerol (HG) is a neutral lipid containing a saturated 16-carbon alkyl chain ether and an uncharged headgroup.

Aplicação

1-C16 Ether MG or 1-O-hexadecyl-sn-glycerol (HG) might be used to study its effect on target gene expression in HepG2 cells. It might also be used to promote plasmalogen biosynthesis in lymphoblasts derived from Barth syndrome (BTHS) patients.

Ações bioquímicas/fisiológicas

1-C16 Ether MG or 1-O-hexadecyl-sn-glycerol (HG) acts as a precursor for plasma plasmalogen (PI) biosynthesis. It is essential for maintaining the plasmalogen levels in cell lines.

Embalagem

20 mL Clear Glass Screw Cap Vial (999971P-250mg)

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

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


Certificados de análise (COA)

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Santosh Phuyal et al.
The Journal of biological chemistry, 290(7), 4225-4237 (2014-12-19)
Exosomes are vesicles released by cells after fusion of multivesicular bodies with the plasma membrane. In this study, we have investigated whether ether lipids affect the release of exosomes in PC-3 cells. To increase the cellular levels of ether lipids
José Carlos Bozelli et al.
Biochimica et biophysica acta. Molecular and cell biology of lipids, 1865(6), 158677-158677 (2020-03-04)
In Barth syndrome (BTHS) mutations in tafazzin leads to changes in both the quantities and the molecular species of cardiolipin (CL), which are the hallmarks of BTHS. Contrary to the well-established alterations in CL associated with BTHS; recently a marked
Akira Abe et al.
Journal of lipid research, 48(10), 2255-2263 (2007-07-14)
A novel lysosomal phospholipase A(2) (LPLA2) with specificity toward phosphatidylethanolamine and phosphatidylcholine was previously purified and cloned. LPLA2 transfers sn-1 or sn-2 acyl groups of phospholipids to the C1 hydroxyl of the short-chain ceramide N-acetylsphingosine (NAS) under acidic conditions. The

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