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Merck
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Documentos Principais

18448

Sigma-Aldrich

N-Stearoyl-D-sphingosine

≥98.0% (TLC)

Sinônimo(s):

Cer(d18:1/18:0), (2S,3R,4E)-2-(Stearoylamino)-4-octadecene-1,3-diol, N-Octadecanoyl-D-sphingosine, N-Stearoyl-D-erythro-sphingosine, N-[(1S,2R,3E)-2-Hydroxy-1-(hydroxymethyl)-3-heptadecen-1-yl]octadecanamide, C18 Ceramide (d18:1/18:0), C18-Ceramide

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About This Item

Fórmula empírica (Notação de Hill):
C36H71NO3
Número CAS:
Peso molecular:
565.95
Beilstein:
1717539
Número MDL:
Código UNSPSC:
12352211
ID de substância PubChem:
NACRES:
NA.85

Nível de qualidade

Ensaio

≥98.0% (TLC)

Formulário

powder or crystals

composição

carbon content, 76.40%
hydrogen content, 12.64%
nitrogen content, 2.47%

grupo funcional

amide

tipo de lipídio

sphingolipids

Condições de expedição

wet ice

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

OC[C@]([H])(NC(CCCCCCCCCCCCCCCCC)=O)[C@]([H])(O)/C=C/CCCCCCCCCCCCC

InChI

1S/C36H71NO3/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/h29,31,34-35,38-39H,3-28,30,32-33H2,1-2H3,(H,37,40)/b31-29+/t34-,35+/m0/s1

chave InChI

VODZWWMEJITOND-NXCSZAMKSA-N

Categorias relacionadas

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable


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Birgit Plochberger et al.
Langmuir : the ACS journal of surfaces and colloids, 26(22), 17322-17329 (2010-10-15)
We investigated the mobility and phase-partitioning of the fluorescent oxidized phospholipid analogue 1-palmitoyl-2-glutaroyl-sn-glycero-3-phospho-N-Alexa647-ethanolamine (PGPE-Alexa647) in supported lipid bilayers. Compared to the conventional phospholipid dihexadecanoylphosphoethanolamine (DHPE)-Bodipy we found consistently higher diffusion constants. The effect became dramatic when immobile obstacles were inserted
M Mirzaian et al.
Clinica chimica acta; international journal of clinical chemistry, 466, 178-184 (2017-01-17)
Free sphingoid bases (lysosphingolipids) of primary storage sphingolipids are increased in tissues and plasma of several sphingolipidoses. As shown earlier by us, sphingoid bases can be accurately quantified using UPLC-ESI-MS/MS, particularly in combination with identical
Erik B Watkins et al.
Biophysical journal, 114(5), 1103-1115 (2018-03-15)
The influence of carbohydrate structure on the ordering of glycosphingolipids (GSLs) and surrounding phospholipids was investigated in monolayers at the air-water interface. Binary mixtures composed of GSLs, chosen to span a range of carbohydrate complexity, and zwitterionic dipalmitoylphosphatidylcholine phospholipid, were
Alice Gualerzi et al.
Scientific reports, 7(1), 9820-9820 (2017-08-31)
Extracellular vesicles (EVs) from mesenchymal stromal cells (MSC) are emerging as valuable therapeutic agents for tissue regeneration and immunomodulation, but their clinical applications have so far been limited by the technical restraints of current isolation and characterisation procedures. This study
Emile Zakiev et al.
Journal of clinical lipidology, 13(3), 468-480 (2019-04-21)
Familial apolipoprotein A-I (apoA-I) deficiency (FAID) involving low levels of both apoA-I and high-density lipoprotein (HDL) cholesterol is associated with accelerated atherosclerosis. The objective of this study was to define distinctive patterns in the lipidome of HDL subpopulations in FAID

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