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Merck
CN

860871P

Avanti

C24:1 Mono-sulfo galactosyl (alpha) ceramide (d18:1/24:1)

Avanti Research™ - A Croda Brand

别名:

3-O-Sulfo-D-galactosyl-α1,1′-N-Nervonoyl-D-erythro-sphingsoine (ammonium salt), (synthetic)

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关于此项目

经验公式（希尔记法）:
C48H94N2O11S
化学文摘社编号:
2260670-38-8
分子量:
907.33
UNSPSC代码:
12352211
NACRES:
NA.25

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产品名称

C24:1 Mono-sulfo galactosyl (alpha) ceramide (d18:1/24:1), Avanti Research™ - A Croda Brand 860871P, powder

方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 1 mg (860871P-1mg)

制造商/商品名称

Avanti Research™ - A Croda Brand 860871P

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(CCCCCCCCCCCCC/C=C\CCCCCCCC)=O)CO[C@@H](O1)[C@H](O)[C@@H](OS([O-])(=O)=O)[C@H]([C@H]1CO)O.[NH4+]

InChI

1S/C48H91NO11S.H3N/c1-3-5-7-9-11-13-15-17-18-19-20-21-22-23-24-26-28-30-32-34-36-38-44(52)49-41(42(51)37-35-33-31-29-27-25-16-14-12-10-8-6-4-2)40-58-48-46(54)47(60-61(55,56)57)45(53)43(39-50)59-48;/h17-18,35,37,41-43,45-48,50-51,53-54H,3-16,19-34,36,38-40

InChI key

MQKRPROAXITSNY-BVRPAXLXSA-N

相关类别

一般描述

C24:1 Mono-sulfo galactosyl (a) ceramide (d18:1/24:1), also known as 3-O-Sulfo-D-galactosyl-a 1,1′-N-Nervonoyl-D-erythro-sphingsoine, is a synthetic sulfatide that belongs to the class of glycosphingolipids.

生化/生理作用

Sulfatides play a crucial role in various cellular processes such as protein trafficking, signal transduction and neuronal cell differentiation. Accumulation of 3-O-Sulfogalactosylceramides (sulfatides), due to the deficiency of arylsulfatase A, leads to genetic disease metachromatic leukodystrophy.

包装

5 mL Amber Glass Screw Cap Vial (860871P-1mg)

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)

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Analysis of complex lipidomes
Uphoff A, et al.
Medical Applications of Mass Spectrometry (2008)
Yanli Cui et al.
Glycoconjugate journal, 25(2), 147-155 (2007-08-19)
3-O-Sulfogalactosylceramides (sulfatides) accumulate in the genetic disease metachromatic leukodystrophy which is due to a defect in the catabolic enzyme, arylsulfatase A. Clinical diagnosis is usually confirmed by in vitro enzymatic deficiency of arylsulfatase A activity. The diagnosis may be complicated

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