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LM2000

Avanti

Sphingosine (d17:1)

Avanti Research™ - A Croda Brand LM2000, ethanol solution

Synonyme(s) :

heptadeca-sphing-4-enine

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About This Item

Formule empirique (notation de Hill):
C17H35NO2
Numéro CAS:
6918-48-5
Poids moléculaire :
285.47
Code UNSPSC :
12352211
Nomenclature NACRES :
NA.25

Forme

ethanol solution

Conditionnement

pkg of 1 × 1 mL (LM2000-1EA)

Fabricant/nom de marque

Avanti Research™ - A Croda Brand LM2000

Concentration

~10 μg/mL (Refer to C of A for lot specific concentration.)

Conditions d'expédition

dry ice

Température de stockage

−20°C

Chaîne SMILES 

OC[C@@](N)([H])[C@]([H])(O)/C=C/CCCCCCCCCCCC

InChI

1S/C17H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17(20)16(18)15-19/h13-14,16-17,19-20H,2-12,15,18H2,1H3/b14-13+/t16-,17+/m0/s1

Clé InChI

RBEJCQPPFCKTRZ-LHMZYYNSSA-N

Catégories apparentées

Application

Sphingosine (d17:1) or heptadeca-sphing-4-enine might be used as an internal standard for the identification of long chain bases (LCBs) in Colletotrichum gloeosporioides mycelia. It is also used as an internal standard for sample preparation and LC-MS/MS analysis for sphingolipids.

Conditionnement

2 mL Amber Glass Sealed Ampule (LM2000-1EA)

Informations légales

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictogrammes

FlameExclamation mark
GHS02,GHS07

Mention d'avertissement

Danger

Mentions de danger

H225,H319

Classification des risques

Eye Irrit. 2 - Flam. Liq. 2

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

55.4 °F - closed cup

Point d'éclair (°C)

13.0 °C - closed cup

Certificats d'analyse (COA)

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Yimei Huang et al.
Frontiers in microbiology, 10, 1016-1016 (2019-06-06)
Fungal glucosylceramide plays important role in cell division, hyphal formation and growth, spore germination and the modulation of virulence and has recently been considered as target for small molecule inhibitors. In this study, we characterized CgGCS, a protein encoding a
Christopher M Adams et al.
The Journal of biological chemistry, 279(50), 52772-52780 (2004-09-29)
The current paper demonstrates that cholesterol and its hydroxylated derivative, 25-hydroxycholesterol (25-HC), inhibit cholesterol synthesis by two different mechanisms, both involving the proteins that control sterol regulatory element-binding proteins (SREBPs), membrane-bound transcription factors that activate genes encoding enzymes of lipid
Claudia Rossi et al.
International journal of molecular sciences, 19(11) (2018-11-18)
Multiple sclerosis (MuS) is an autoimmune disease of the central nervous system characterized by neuroinflammation, neurodegeneration, and degradation of the myelin sheath. Epidemiological studies have shown that the female gender is more susceptible than the male gender to MuS development
Veera Venkata Ratnam Bandaru et al.
BMC neuroscience, 15, 137-137 (2014-12-30)
Cholesterol metabolism is important for the maintenance of myelin and neuronal membranes in the central nervous system. Blood concentrations of the brain specific cholesterol metabolite 24S-hydroxysterol to the peripheral metabolite 27-hydroxycholesterol may be useful surrogate markers for neurodegenerative diseases including
Rosamaria Lappano et al.
PloS one, 6(1), e16631-e16631 (2011-02-10)
The hydroxylated derivatives of cholesterol, such as the oxysterols, play important roles in lipid metabolism. In particular, 25-hydroxycholesterol (25 HC) has been implicated in a variety of metabolic events including cholesterol homeostasis and atherosclerosis. 25 HC is detectable in human
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