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Merck
CN

870602P

Avanti

PGPC

Avanti Research - A Croda Brand 870602P, powder

别名:

1-棕榈酰-2-戊二酰-sn-甘油-3-磷酸胆碱

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About This Item

经验公式(希尔记法):
C29H56NO10P
CAS号:
分子量:
609.73
UNSPSC代码:
12352211
NACRES:
NA.25

形式

powder

包装

pkg of 1 × 1 mg (870602P-1mg)
pkg of 1 × 5 mg (870602P-5mg)

制造商/商品名称

Avanti Research - A Croda Brand 870602P

运输

dry ice

储存温度

−20°C

SMILES字符串

[O-]P(OCC[N+](C)(C)C)(OC[C@]([H])(OC(CCCC(O)=O)=O)COC(CCCCCCCCCCCCCCC)=O)=O

一般描述

1-棕榈酰-2-戊二酰-sn-甘油-3-磷酸胆碱(PGPC) 是氧化修饰的低密度脂蛋白(oxLDL) 的一种成分。它是由一种主要的低密度脂蛋白(LDL) 磷脂 1-棕榈酰-2-戊二酰-sn-甘油-3-磷酸胆碱(PGPC)的非酶氧化合成的。

应用

1-棕榈酰-2-戊二酰-sn-甘油-3-磷酸胆碱(PGPC) 已被用于使用单分子显微镜研究其对质膜纳米平台的影响。

生化/生理作用

1-棕榈酰-2-戊二酰-sn-甘油-3-磷酸胆碱(PGPC)在培养的血管平滑肌细胞和巨噬细胞中充当炎症、增殖或凋亡的诱导剂。它在动脉粥样硬化病变中积累。

包装

5 mL透明玻璃密封安瓿(870602P-1mg)
5 mL透明玻璃密封安瓿(870602P-5mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids


分析证书(COA)

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The oxidized phospholipids POVPC and PGPC inhibit growth and induce apoptosis in vascular smooth muscle cells
Fruhwirth GO, et al.
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1761(9), 1060-1069 (2006)
The role of high-density lipoproteins in oxidation and inflammation
Van Lenten B, et al.
Trends in Cardiovascular Medicine, 11(3-4), 155-161 (2001)
Oxidized phospholipids inhibit the formation of cholesterol-dependent plasma membrane nanoplatforms
Brameshuber M, et al.
Biophysical Journal, 110(1), 205-213 (2016)
Alexandra Moumtzi et al.
Journal of lipid research, 48(3), 565-582 (2006-12-01)
Lipid oxidation is now thought to be an initiating and sustaining event in atherogenesis. Oxidatively fragmented phospholipids, namely 1-palmitoyl-2-glutaroyl-sn-glycero-3-phosphocholine (PGPC) and 1-palmitoyl-2-(5-oxovaleroyl)-sn-glycero-3-phosphocholine (POVPC), present in minimally modified LDL and atherosclerotic lesions, have been reported to elicit a wide range of
Marco Di Gioia et al.
Nature immunology, 21(1), 42-53 (2019-11-27)
Pathogen-associated molecular patterns (PAMPs) have the capacity to couple inflammatory gene expression to changes in macrophage metabolism, both of which influence subsequent inflammatory activities. Similar to their microbial counterparts, several self-encoded damage-associated molecular patterns (DAMPs) induce inflammatory gene expression. However

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