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860431P

Avanti

C16 Galactosyl(α) Ceramide (d18:1/16:0)

D-galactosyl-α-1,1′ N-palmitoyl- D-erythro-sphingosine, powder

Sinónimos:

C16 α-D-galactosyl ceramide; N-(hexadecanoyl)-1-α-galactosyl-sphing-4-enine

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About This Item

Fórmula empírica (notación de Hill):
C40H77NO8
Número de CAS:
2260795-77-3
Peso molecular:
700.04
UNSPSC Code:
12352211
NACRES:
NA.25

assay

>99% (TLC)

form

powder

packaging

pkg of 1 × 5 mg (860431P-5mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand 860431P

lipid type

sphingolipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@]([C@@]([H])(/C=C/CCCCCCCCCCCCC)O)(NC(CCCCCCCCCCCCCCC)=O)CO[C@@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO)O

Application

C16 Galactosyl(α) Ceramide (d18:1/16:0) or α -GalCer (d18:1/16:0) is suitable for use as a hexosylceramides (HexCers) standard in high-performance thin layer chromatography (HPTLC).

Packaging

5 mL Amber Glass Screw Cap Vial (860431P-5mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class

11 - Combustible Solids

flash_point_f

No data available

flash_point_c

No data available

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Kathrin M Engel et al.
Biomolecules, 10(2) (2020-01-26)
The lipid composition of sperm membranes is crucial for fertilization and differs among species. As the evolution of internal fertilization modes in fishes is not understood, a comparative study of the sperm lipid composition in freshwater representatives of externally and
Diastereomer-specific quantification of bioactive hexosylceramides from bacteria and mammals
Von Gerichten J, et al.
Journal of Lipid Research, 58(6), 1247-1258 (2017)
Guang-Yi Dai et al.
The Journal of biological chemistry, 295(3), 717-728 (2019-12-11)
Cellular membranes contain many lipids, some of which, such as sphingolipids, have important structural and signaling functions. The common sphingolipid glucosylceramide (GlcCer) is present in plants, fungi, and animals. As a major plant sphingolipid, GlcCer is involved in the formation
Johanna von Gerichten et al.
Journal of lipid research, 58(6), 1247-1258 (2017-04-05)
Mammals synthesize, cell-type specifically, the diastereomeric hexosylceramides, β-galactosylceramide (GalCer) and β-glucosylceramide (GlcCer), which are involved in several diseases, such as sphingolipidosis, diabetes, chronic kidney diseases, or cancer. In contrast, Bacteroides fragilis, a member of the human gut microbiome, and the

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