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Merck
CN

850465C

Avanti

18:0-16:0 PC

Avanti Research - A Croda Brand

别名:

1-octadecanoyl-2-hexadecanoyl-sn-glycero-3-phosphocholine; SPPC; PC(18:0/16:0)

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关于此项目

经验公式(希尔记法):
C42H84NO8P
化学文摘社编号:
分子量:
762.09
UNSPSC代码:
12352211
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产品名称

18:0-16:0 PC, 1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine, chloroform

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 2.5 mL (850465C-25mg)

制造商/商品名称

Avanti Research - A Croda Brand 850465C

浓度

10 mg/mL (850465C-25mg)

脂质类型

phospholipids
cardiolipins

运输

dry ice

储存温度

−20°C

一般描述

Phosphatidylcholines (PCs) are amphipathic molecules, which accounts for approximately 40−50% of the total cellular phospholipids. 18:0-16:0 PC (1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine) is an asymmetric lipid.

应用

18:0-16:0 PC (1-stearoyl-2-palmitoyl-sn-glycero-3-phosphocholine) may be used:
  • in bilayer membranes to study the thermodynamic properties of phase transitions
  • as a carrier in unilamellar vesicles to evaluate the fragmentation of hydroperoxy endoperoxide 13-HP-Endo-PC in a model membrane
  • as a lipid standard in liquid chromatography−mass spectrometry analysis

生化/生理作用

Phosphatidylcholine (PC) has the ability to block the penetrance of bacteria by acting as a surfactant.

包装

5 mL Clear Glass Sealed Ampule (850465C-25mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3

靶器官

Central nervous system

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

闪点(°F)

does not flash

闪点(°C)

does not flash

法规信息

新产品
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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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Inflammatory Bowel Disease
Parian AM, et al.
Integrative Medicine, 501-516 (2018)
Xiaodong Gu et al.
Chemical research in toxicology, 24(7), 1080-1093 (2011-05-17)
Biologically active phospholipids that incorporate an oxidatively truncated acyl chain terminated by a γ-hydroxyalkenal are generated in vivo. The γ-hydroxyalkenal moiety protrudes from lipid bilayers like whiskers that serve as ligands for the scavenger receptor CD36, fostering endocytosis, e.g., of
Masaki Goto et al.
Biochimica et biophysica acta, 1778(4), 1067-1078 (2008-01-15)
The bilayer phase transitions of palmitoylstearoyl-phosphatidylcholine (PSPC), diheptadecanoyl-PC (C17PC) and stearoylpalmitoyl-PC (SPPC) which have the same total carbon numbers in the two acyl chains were observed by differential scanning calorimetry and high-pressure optical method. As the temperature increased, these bilayers
Simon Becher et al.
Analytical chemistry, 90(19), 11486-11494 (2018-09-11)
Phosphatidylcholines are the major phospholipid component of most eukaryotic cell membranes. Phosphatidylcholines have been shown to actively participate in regulatory and metabolic processes. Dysfunctional metabolic processes have been linked to human disease and can result in altered phosphatidylcholine structural features
Jelske N van der Veen et al.
Biochimica et biophysica acta. Biomembranes, 1859(9 Pt B), 1558-1572 (2017-04-16)
Phosphatidylcholine (PC) and phosphatidylethanolamine (PE) are the most abundant phospholipids in all mammalian cell membranes. In the 1950s, Eugene Kennedy and co-workers performed groundbreaking research that established the general outline of many of the pathways of phospholipid biosynthesis. In recent

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