Basic information Safety Supplier Related

C6 L-erythro Ceramide (d18:1/6:0)

Basic information Safety Supplier Related

C6 L-erythro Ceramide (d18:1/6:0) Basic information

Product Name:
C6 L-erythro Ceramide (d18:1/6:0)
Synonyms:
  • C6 L-erythro Ceramide (d18:1/6:0)
  • Hexanoyl-L-erythro-sphingosine
  • Hexanamide, N-[(1R,2S,3E)-2-hydroxy-1-(hydroxymethyl)-3-heptadecen-1-yl]-
  • N-[(1R,2S,3E)-2-hydroxy-1-(hydroxymethyl)-3-heptadecen-1-yl]-hexanamide
CAS:
189894-78-8
MF:
C24H47NO3
MW:
397.63
Mol File:
189894-78-8.mol
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C6 L-erythro Ceramide (d18:1/6:0) Chemical Properties

Boiling point:
574.7±50.0 °C(Predicted)
Density 
0.946±0.06 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
Chloroform: Soluble; DMF: 5 mg/ml; DMSO: Soluble; Ethanol: Soluble
form 
A solid
pka
13.53±0.20(Predicted)
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C6 L-erythro Ceramide (d18:1/6:0) Usage And Synthesis

Description

C6 L-erythro Ceramide is a bioactive sphingolipid and cell-permeable analog of naturally occurring ceramides.1,2 It is metabolized by ceramide glucosyltransferase to form C6 L-erythro glucosylceramide. C6 L-erythro Ceramide is cytotoxic to U937 cells (IC50 = 18 μM).3

References

1. Schwarz, A., and Futerman, A.H. Distinct roles for ceramide and glucosylceramide at different stages of neuronal growth J. Neurosci. 17(9),2929-2938(1997).
2. Paul, P., Kamisaka, Y., Marks, D.L., et al. Purification and characterization of UDP-glucose: Ceramide glucosyltransferase from rat liver Golgi membranes Curr. Opin. Struct. Biol. 271(4),2287-2293(1996).
3. Chang, Y.-T., Choi, J., Ding, S., et al. The synthesis and biological characterization of a ceramide library J. Am. Chem. Soc. 124(9),1856-1857(2002).

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