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MilliporeSigma

999971P

Avanti

1-C16 Ether MG

Avanti Polar Lipids 999971P, powder

Sinónimos:

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

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About This Item

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

form

powder

packaging

pkg of 1 × 250 mg (999971P-250mg)

manufacturer/tradename

Avanti Polar Lipids 999971P

lipid type

phospholipids
neutral lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[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

InChI key

OOWQBDFWEXAXPB-UHFFFAOYSA-N

General description

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.

Application

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.

Biochem/physiol Actions

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.

Packaging

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

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (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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