860456 | N-C16-deoxysphingosine

N-palmitoyl-1-deoxysphingosine (m18:1/16:0)


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N-C16-deoxysphingosine

N-C16-deoxysphingosine

N-palmitoyl-1-deoxysphingosine (m18:1/16:0)

Hygroscopic
No
Light Sensitive
No
Molecular Formula
C34H67NO2
Percent Composition
C 78.25%, H 12.94%, N 2.68%, O 6.13%
Purity
>99%
Stability
1 Years
Storage Temperature
-20°C
CAS Number
1246298-56-5
CAS Registry Number is a Registered Trademark of the American Chemical Society
Formula Weight
521.901
Exact Mass
521.517
Synonyms
N-hexadecanoyl-1-deoxysphing-4-enine (m18:1/16:0)
N-C16-1-deoxyCer
110994

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. PMID: 18499644; PMCID: PMC2444003.

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. PMID: 19095642; PMCID: PMC2643501.

PubMed ID: 19095642