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