N,N-Dihexyl-D-erythro-sphingosine/ml 1ml ethanolN,N-Dihexyl-D-erythro-sphingosine/ml 1ml ethanol
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N,N-Dihexyl-D-erythro-sphingosine/ml 1ml ethanol

Sphingosine with tertiary amine group

N,N-Dihexyl-D-erythro-sphingsosine is an unnatural analog of the vital sphingolipid ceramide. Ceramide functions as a precursor in the synthesis of sphingomyelin, complex glycosphingolipids, and free sphingosine and it exerts numerous biological effects, including induction of cell maturation, cell cycle arrest, terminal cell differentiation, cell senescence, and cell death.1 Instead of the normal fatty acid acylated to sphingosine N,N-Dihexyl-D-erythro-sphingsosine contains two hexyl groups making it a tertiary amine rather than secondary. Ceramide analogs, such as N,N-Dihexyl-D-erythro-sphingsosine, are able to induce an a increase in ceramide levels in cells, leading to apoptosis, and may be useful in treating certain diseases.2 N-Hexyl-glucosylceramide is a potent inhibitor of glucosylceramidase, the enzyme responsible for cleaving glucose from glucosylceramide.3
Cat# Size Price Qty Buy
1896 5 mg/ml 1ml £210.94

Additional Information

Property Value or Rating
Product Size 5 mg/ml 1ml
Manufacturer Matreya, LLC
Empirical Formula C30H61NO2
Formula Weight 467.8
Solvent ethanol
Source synthetic
Purity 95%
Analytical Methods TLC
Natural Source Synthetic
Solubility chloroform, methanol, ethanol
Physical Appearance A 5 mg/ml liquid in ethanol
Storage -20°C
References

1. N. S. Radin, “Killing tumours by ceramide-induced apoptosis: a critique of available drugs” Biochemical Journal, Vol. 371 pp. 243-256, 2003 
2. J. Erickson and N. Radin “N-Hexyl-0-glucosyl sphingosine, an inhibitor of glucosyl ceramide, beta-glucosidase” Journal of Lipid Research, Vol. 14 pp. 133-137, 1973 
3. S. Gatt et al. “Synthetic, non-natural sphingolipid analogs inhibit the biosynthesis of cellular sphingolipids, elevate ceramide and induce apoptotic cell death” Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, Vol. 1633(3) pp. 161-169, 2003

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