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C18 Globotriaosylceramide (d18:1/18:0)

C18 Globotriaosylceramide (d18:1/18:0) ??? ???
?? ??:
69283-33-6
???:
C18 Globotriaosylceramide (d18:1/18:0)
???(??):
Octadecanoyl-ceramide trihexoside;N-Octadecanoyl-ceramide trihexoside;C18 Globotriaosylceramide (d18:1/18:0);Octadecanamide, N-[(1S,2R,3E)-1-[[(O-α-D-galactopyranosyl-(1→4)-O-β-D-galactopyranosyl-(1→4)-β-D-glucopyranosyl)oxy]methyl]-2-hydroxy-3-heptadecen-1-yl]-
CBNumber:
CB84666974
???:
C54H101NO18
??? ??:
1052.37564
MOL ??:
69283-33-6.mol

C18 Globotriaosylceramide (d18:1/18:0) ??

?? ?
1132.1±65.0 °C(Predicted)
??
1.22±0.1 g/cm3(Predicted)
?? ??
Store at -20°C
???
Chloroform:Methanol (2:1): Soluble; DMSO: Soluble; Methanol: Warmed
??? ??
??
?? ?? (pKa)
12.76±0.70(Predicted)

??

C18 Globotriaosylceramide (d18:1/18:0) C??? ??, ??, ??

??

C18 globotriaosylceramide is an endogenous sphingolipid found in mammalian cell membranes that is synthesized from lactosylceramide . It inhibits aggregation of human neutrophils induced by phorbol 12-myristate 13-acetate (PMA; 10008014) when used at a concentration of 1 μM. C18 globotriaosylceramide acts as a receptor for Shiga toxin in B cell-derived Raji cells and THP-1 monocytes. It accumulates in the brain, heart, kidney, liver, lung, and spleen in a mouse model of Fabry disease, a lysosomal storage disorder characterized by a deficiency in the enzyme α-galactosidase A. C18 globotriaosylceramide also accumulates in endothelial cells, pericytes, vascular smooth muscle cells, renal epithelial cells, dorsal ganglia neuronal cells, and myocardial cells in patients with Fabry disease. [Matreya, LLC. Catalog No. 1529]

C18 Globotriaosylceramide (d18:1/18:0) ?? ?? ? ???

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C18 Globotriaosylceramide (d18:1/18:0) ?? ??

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