C24-Ceramide
C24-Ceramide Basic information
- Product Name:
- C24-Ceramide
- Synonyms:
-
- C24-D-ERYTHRO-CERAMIDE
- C24 CERAMIDE
- LIGNOCERIC CERAMIDE
- TETRACOSENAMIDE
- N-TETRACOSANOYLSPHINGOSINE
- N-TETRACOSANOYL-D-ERYTHRO-SPHINGOSINE
- N-MYRISTOYL-D-ERYTHRO-SPHINGOSINE
- N-MYRISTOYL-D-SPHINGOSINE
- CAS:
- 34435-05-7
- MF:
- C42H83NO3
- MW:
- 650.11
- Product Categories:
-
- Mixed Fatty Acids
- Activators
- Fatty Acid Derivatives & Lipids
- Glycerols
- Inhibitors
- Protein Kinase Inhibitors and Activators
- Mol File:
- 34435-05-7.mol
C24-Ceramide Chemical Properties
- Melting point:
- 94-96
- Boiling point:
- 750.0±60.0 °C(Predicted)
- Density
- 0.906±0.06 g/cm3(Predicted)
- storage temp.
- -20°C Freezer
- solubility
- Chloroform (Sparingly)
- form
- Solid
- pka
- 13.54±0.20(Predicted)
- color
- White to Off-White
MSDS
- Language:English Provider:ACROS
C24-Ceramide Usage And Synthesis
Description
Production of ceramide occurs upon hydrolysis of sphingomyelin by a specific isoform of PLC, appropriately named sphingomyelinase. C24 Ceramide (d18:1/24:0) is one of the most abundant naturally occurring ceramides. Ceramides mediate many diverse biological activities, as has been demonstrated in studies utilizing cell-
Chemical Properties
Crystalline Solid
Uses
Production of ceramide occurs upon hydrolysis of sphingomyelin by a specific isoform of phospholipase C, appropriately named sphingomyelinase.
Definition
ChEBI: N-tetracosanoylsphingosine is a N-acylsphingosine in which the ceramide N-acyl group is specified as tetracosanoyl. It has a role as a mouse metabolite. It is a N-acylsphingosine, a Cer(d42:1) and a N-(very-long-chain fatty acyl)-sphingoid base. It is functionally related to a tetracosanoic acid.
References
[1] MING GU . Ceramide Profiling of Complex Lipid Mixtures by Electrospray Ionization Mass Spectrometry[J]. Analytical biochemistry, 1997, 244 2: Pages 347-356. DOI: 10.1006/abio.1996.9915
[2] R B CLAYTON. Stimulation of erythroblast maturation in vitro by sphingolipids.[J]. Journal of Lipid Research, 1974, 15 6: 557-562.
[3] W KRIVIT S H. Identification and quantitation of free ceramides in human platelets.[J]. Journal of Lipid Research, 1972, 13 4: 525-530.
[4] TESTI R. Sphingomyelin breakdown and cell fate[J]. Trends in Biochemical Sciences, 1996, 21 12: Pages 468-471. DOI: 10.1016/s0968-0004(96)10056-6
[5] N AUGé. The sphingomyelin-ceramide signaling pathway is involved in oxidized low density lipoprotein-induced cell proliferation.[J]. The Journal of Biological Chemistry, 1996, 271 32: 19251-19255. DOI: 10.1074/jbc.271.32.19251
[6] T I GUDZ C L H K Y Tserng. Direct inhibition of mitochondrial respiratory chain complex III by cell-permeable ceramide.[J]. The Journal of Biological Chemistry, 1997, 272 39: 24154-24158. DOI: 10.1074/jbc.272.39.24154
C24-CeramideSupplier
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