您的位置:首页>>分析化学>>脂类分析标准品>>1848 N-己酰-L-赤式-鞘氨醇 N-Hexanoyl-L-erythro-sphingosine
Cat. Number
1848
Chemical Name
1848 N-己酰-L-赤式-鞘氨醇 N-Hexanoyl-L-erythro-sphingosine
Mol. Formula
C24H47NO3
Mol. Weight
398
Qty 1
1mg
Appearance
solid
Application Notes
98+%,TLC; identity confirmed by MS
Synonym
N-C6:0-L-erythro-Ceramide
Solubility
chloroform, ethanol, DMSO, DMF (up to 5mg/ml)
Storage condition
-20℃
References

Application Notes:

This product is the L-erythro stereoisomer of natural D-erythro-hexanoyl ceramide. L-erythro ceramides are inactive in some ceramide functions, have different activities in other functions, and exhibit the same activity in yet other functions. Lerythro- N-acetyl ceramide has been shown to induce accumulation of greater levels of sphingosine than in control cells.1 Generation of endogenous long-chain ceramide can be induced by exogenous short chain D-erythro-hexanoyl-ceramide but not by non-natural L-erythro-hexanoyl-ceramide.2 Other examples of functions demonstrated by D-erythro, but not Lerythro, ceramides are several key downstream biological activities such as growth inhibition, cell cycle arrest, and modulation of telomerase activity.2 Some viruses require the presence of ceramide in a membrane to be able to fuse to that membrane and it has been demonstrated that only D-erythro ceramide, and not L-erythro or D- or L-threo ceramides, supports the viral fusion.3

References: 
1. Y. Lee et al. “Sphingolipid metabolic changes during chiral C2-ceramides induced apoptosis in human leukemia cells” Arch Pharm Res, vol. 24 pp. 144- 149, 2001 
2. Y. Hannun et al. “Biochemical Mechanisms of the Generation of Endogenous Long Chain Ceramide in Response to Exogenous Short Chain Ceramide in the A549 Human Lung Adenocarcinoma Cell Line” The Journal of Biological Chemistry, vol. 277 pp. 12960–12969, 2002 
3. J. Wilschut et al. “Sphingolipids Activate Membrane Fusion of Semliki Forest Virus in a Stereospecific Manner” Biochemistry, vol. 34 pp. 10319-10324, 1995

在线咨询 联系方式 二维码

服务热线

021-60498804

扫一扫,关注我们