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Merck
CN

870729P

Avanti

25:0 Coenzyme A

Avanti Research - A Croda Brand 870729P, powder

别名:

pentacosanoyl Coenzyme A (ammonium salt)

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About This Item

经验公式(希尔记法):
C46H93N10O17P3S
分子量:
1183.27
UNSPSC代码:
12352211
NACRES:
NA.25

表单

powder

包装

pkg of 1 × 5 mg (870729P-5mg)

制造商/商品名称

Avanti Research - A Croda Brand 870729P

应用

lipidomics

脂质类型

coenzymes

运输

dry ice

储存温度

−20°C

SMILES字符串

O[C@@](C(NCCC(NCCSC(CCCCCCCCCCCCCCCCCCCCCCCC)=O)=O)=O)(C(C)(COP([O-])(OP([O-])(OC[C@H]([C@H]1OP([O-])(O)=O)O[C@H]([C@@H]1O)N2C3=C(C(N)=NC=N3)N=C2)=O)=O)C)[H].[NH4+].[NH4+].[NH4+]

InChI key

YJOJYMDYLIGHLQ-SLTOUGITSA-N

一般描述

25:0 Coenzyme A or pentacosanoyl coenzyme A is a long chain fatty acyl-CoA. Fatty acyl-CoAs is produced from de-novo fatty acid biosynthesis and the reprocessing of pre-existing fatty acids.
25:0 Coenzyme A, also known as pentacosanoyl coenzyme A, is a coenzyme derivative of pentacosanoic acid.

应用

25:0 Coenzyme A has been used as a constituent of the internal standard mixture in liquid chromatography-electrospray ionization tandem mass spectrometry (LC/ESI-MS/MS).
25:0 Coenzyme A or pentacosanoyl Coenzyme A has been used as a substrate for 1-acylglycerol-3-phosphate-O-acyltransferase 11 (AGPAT11) enzyme. It has also been used as an internal standard to quantify fatty acyl CoA extracted from human embryonic kidney 293 cells.

生化/生理作用

Fatty acyl-CoA plays a vital role in various cellular processes including, energy metabolism, the biosynthesis and recycling of complex lipids, the posttranslational modification of proteins and the regulation of gene expression. In addition, it facilitates most of the fatty acid modification reactions. 25:0 coenzyme A might function as a precursor of sphingolipids. Alterations in the fatty acyl-CoA metabolism leads to obesity, cardiovascular disease, diabetes mellitis and cancer.

包装

5 mL Amber Glass Screw Cap Vial (870729P-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

法规信息

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Fatty acid oxidation and control of food intake
Leonhardt M and Langhans W
Physiology & Behavior, 83(4), 645-651 (2004)
Christopher A Haynes et al.
Journal of lipid research, 52(8), 1583-1594 (2011-05-19)
This study describes the use of a stable-isotope labeled precursor ([U-¹³C]palmitate) to analyze de novo sphingolipid biosynthesis by tandem mass spectrometry. It also describes factors to consider in interpreting the data, including the isotope's location (¹³C appears in three isotopomers
Role of fatty acid binding proteins and long chain fatty acids in modulating nuclear receptors and gene transcription
Schroeder F, et al.
Lipids, 43(1), 1-17 (2008)
Quantitation of fatty acyl-coenzyme As in mammalian cells by liquid chromatography-electrospray ionization tandem mass spectrometry
Haynes CA, et al.
Journal of Lipid Research, 49(5), 1113-1125 (2008)
Factors to consider in using [UC] palmitate for analysis of sphingolipid biosynthesis by tandem mass spectrometry
Haynes CA, et al.
Journal of Lipid Research, 52(8), 1583-1594 (2011)

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