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14386

Sigma-Aldrich

N-Oleoyl-D-sphingosine

≥98.0% (TLC)

Sinônimo(s):

Cer(d18:1/18:1(9Z)), (2S,3R,4E)-2-(Oleoylamino)-4-octadecene-1,3-diol, (9Z)-N-[(1S,2R,3E)-2-Hydroxy-1-(hydroxymethyl)-3-heptadecen-1-yl]-9-octadecenamide, N-(cis-9-Octadecenoyl)-D-sphingosine, N-Oleoyl-D-erythro-sphingosine, C18:1 Ceramide (d18:1/18:1(9Z)), C18:1-Ceramide

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About This Item

Fórmula empírica (Notação de Hill):
C36H69NO3
Número CAS:
5966-28-9
Peso molecular:
563.94
Beilstein:
6283861
Código UNSPSC:
12352211
ID de substância PubChem:
329750284
NACRES:
NA.85

Ensaio

≥98.0% (TLC)

Formulário

powder or solid

composição

carbon content, 76.67%
hydrogen content, 12.33%
nitrogen content, 2.48%

tipo de lipídio

sphingolipids

Condições de expedição

wet ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CCCCCCCCCCCCC\C=C\[C@@H](O)[C@H](CO)NC(=O)CCCCCCC\C=C/CCCCCCCC

InChI

1S/C36H69NO3/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-36(40)37-34(33-38)35(39)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,29,31,34-35,38-39H,3-16,19-28,30,32-33H2,1-2H3,(H,37,40)/b18-17-,31-29+/t34-,35+/m0/s1

chave InChI

OBFSLMQLPNKVRW-RHPAUOISSA-N

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de classe de armazenamento

13 - Non Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCBZ5055
BCBW1917
BCBH6566V
BCBH6566

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Rodell C Barrientos et al.
Journal of the American Society for Mass Spectrometry, 30(9), 1609-1620 (2019-07-10)
The role of cationization in the fragmentation behavior of glycoconjugates is amply documented in collisional activation techniques but remains less explored in ozone-induced dissociation mass spectrometry (OzID-MS). OzID-MS has been used to elucidate the location of carbon-carbon double bonds in
Ayman J Aljohani et al.
Molecular vision, 19, 1966-1984 (2013-09-27)
To determine the differential profiles of sphingomyelin, sphingoid base, sphingoid base-1-phosphate and ceramide lipid species and their quantitative differences between control and glaucomatous aqueous humor (AQH) derived from human donors. AQH from control and primary open-angle glaucoma donors was collected
Eric W Miller et al.
Journal of cellular biochemistry, 120(9), 14383-14404 (2019-04-13)
The formin family of proteins contributes to spatiotemporal control of actin cytoskeletal rearrangements during motile cell activities. The FMNL subfamily exhibits multiple mechanisms of linear actin filament formation and organization. Here we report novel actin-modifying functions of FMNL1 in breast
Vivian A Paschoal et al.
Cell metabolism, 31(6), 1173-1188 (2020-05-16)
G protein-coupled receptor 120 (GPR120) and PPARγ agonists each have insulin sensitizing effects. But whether these two pathways functionally interact and can be leveraged together to markedly improve insulin resistance has not been explored. Here, we show that treatment with
Christopher A Mitchell et al.
Lipids in health and disease, 14, 84-84 (2015-08-06)
Mass spectrometry imaging (MSI) is a powerful tool for the study of intact tissue sections. Here, its application to the study of the distribution of lipids in sections of reconstructed living skin equivalents during their development and maturation is described.

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