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860467 | N-C16-desoxymethylsphingosine

N-palmitoyl-1-desoxymethylsphingosine (m17:1/16:0)

N-C16-desoxymethylsphingosine

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N-C16-desoxymethylsphingosine

N-palmitoyl-1-desoxymethylsphingosine (m17:1/16:0)

Data
Hygroscopic
No
Light Sensitive
No
Molecular Formula
C33H65NO2
Percent Composition
C 78.04%, H 12.90%, N 2.76%, O 6.30%
Purity
>99%
Stability
1 Year
Storage Temperature
-20°C
CAS Number
1246298-57-6
CAS Registry Number is a Registered Trademark of the American Chemical Society
Formula Weight
507.875
Exact Mass
507.502
Synonyms
N-hexadecanoyl-1-desoxymethylsphing-3-enine (m17:1/16:0)
N-C16-1-desoxy
MeCer
110995
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References

Wan J, Li J, Bandyopadhyay S, Kelly SL, Xiang Y, Zhang J, Merrill AH Jr, Duan J. Analysis of 1-Deoxysphingoid Bases and Their N-Acyl Metabolites and Exploration of Their Occurrence in Some Food Materials. J Agric Food Chem. 2019 Nov 20;67(46):12953-12961. doi: 10.1021/acs.jafc.9b05708. Epub 2019 Nov 6.

 PubMed ID: 31638789

Pruett ST, Bushnev A, Hagedorn K, Adiga M, Haynes CA, Sullards MC, Liotta DC, Merrill AH Jr. Biodiversity of sphingoid bases ("sphingosines") and related amino alcohols. J Lipid Res. 2008 Aug;49(8):1621-39. doi: 10.1194/jlr.R800012-JLR200. Epub 2008 May 21.

 PubMed ID: 18499644

Zitomer NC, Mitchell T, Voss KA, Bondy GS, Pruett ST, Garnier-Amblard EC, Liebeskind LS, Park H, Wang E, Sullards MC, Merrill AH Jr, Riley RT. Ceramide synthase inhibition by fumonisin B1 causes accumulation of 1-deoxysphinganine: a novel category of bioactive 1-deoxysphingoid bases and 1-deoxydihydroceramides biosynthesized by mammalian cell lines and animals. J Biol Chem. 2009 Feb 20;284(8):4786-95. doi: 10.1074/jbc.M808798200. Epub 2008 Dec 18.

 PubMed ID: 19095642
Certificates of Analysis

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