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Merck
CN

860840P

Avanti

C18(2R-OH) Galactosyl(β) Ceramide

Avanti Research - A Croda Brand

别名:

D-galactosyl-β1-1′-N-[2′′(R)-hydroxystearoyl]-D-erythro-sphingosine

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关于此项目

经验公式(希尔记法):
C42H81NO9
化学文摘社编号:
分子量:
744.09
UNSPSC代码:
12352211
NACRES:
NA.25
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产品名称

C18(2R-OH) Galactosyl(β) Ceramide, Avanti Research - A Croda Brand 860840P, powder

方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 5 mg (860840P-5mg)

制造商/商品名称

Avanti Research - A Croda Brand 860840P

脂质类型

sphingolipids

运输

dry ice

储存温度

−20°C

SMILES字符串

[H][C@](/C=C/CCCCCCCCCCCCC)(O)[C@@]([H])(NC([C@H](O)CCCCCCCCCCCCCCCC)=O)CO[C@H](O1)[C@H](O)[C@@H](O)[C@H]([C@H]1CO)O

InChI

1S/C42H81NO9/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-36(46)41(50)43-34(33-51-42-40(49)39(48)38(47)37(32-44)52-42)35(45)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h28,30,34-40,42,44-49H,3-27,29,31-33H2,1-2H3,(H,43,50)/b30-28+/t34-,35+,36+,37+,38-,39-,40+

InChI key

ONDPKGSAWAOCRS-KCJZCHLQSA-N

一般描述

Galactosyl ceramide is a complex glycosphingolipid, which is a major component of the myelin sheath. It consists of a single galactose residue linked to ceramide.

应用

C18(2R-OH) Galactosyl(β) Ceramide has been used as a standard to study unsaturated glycosphingolipids using the shotgun approach. It has also been used as a lipid standard for matrix-assisted laser desorption ionization (MALDI) analysis.

生化/生理作用

Galactosyl ceramide is essential for normal myelin function and stability.

包装

5 mL Amber Glass Screw Cap Vial (860840P-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

No data available

闪点(°C)

No data available

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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在文件库中查找您最近购买产品的文档。

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Gangliosides in Health and Disease (2018)
Pediatric Neurology (2013)
Matrix-free mass spectrometry imaging of mouse brain tissue sections on silicon nanopost arrays
Fincher JA, et al.
The Journal of Comparative Neurology (2018)
Divalent cation-mediated interaction between cerebroside sulfate and cerebrosides: an investigation of the effect of structural variations of lipids by electrospray ionization mass spectrometry
Koshy KM, et al.
Biophysical Journal, 77(1), 306-318 (1999)
Structural analysis of unsaturated glycosphingolipids using shotgun ozone-induced dissociation mass spectrometry
Barrientos RC, et al.
Journal of the American Society For Mass Spectrometry, 28(11), 2330-2343 (2017)

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