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Merck
CN

850757C

Avanti

磷脂酰乙醇胺(16:0-18:1 PE)

Avanti Polar Lipids

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别名:
1-十六酰-2-(9Z-十八烯酰)-sn-甘油-3-磷酸乙醇胺;POPE;PE(16:0/18:1(9Z));110637
经验公式(希尔记法):
C39H76NO8P
CAS号:
分子量:
718.00
UNSPSC代码:
51191904
NACRES:
NA.25

描述

1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine, chloroform

检测方案

>99% (TLC)

形式

liquid

包装

pkg of 1 × 2.5 mL (850757C-25mg)
pkg of 2 × 20 mL (850757C-1g)
pkg of 2 × 4 mL (850757C-200mg)
pkg of 5 × 4 mL (850757C-500mg)

制造商/商品名称

Avanti Polar Lipids

浓度

10 mg/mL (850757C-25mg)
25 mg/mL (850757C-1g)
25 mg/mL (850757C-200mg)
25 mg/mL (850757C-500mg)

脂质类型

cardiolipins
phospholipids

运输

dry ice

储存温度

−20°C

SMILES字符串

[H][C@@](COP([O-])(OCC[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O

InChI

1S/C39H76NO8P/c1-3-5-7-9-11-13-15-17-18-20-22-24-26-28-30-32-39(42)48-37(36-47-49(43,44)46-34-33-40)35-45-38(41)31-29-27-25-23-21-19-16-14-12-10-8-6-4-2/h17-18,37H,3-16,19-36,40H2,1-2H3,(H,43,44)/b18-17-

InChI key

FHQVHHIBKUMWTI-ZCXUNETKSA-N

应用

16:0-18:1 PE(磷脂酰乙醇胺)作为合成脂质已用于制备脂质体。

包装

30 mL带螺旋盖的琥珀色窄口玻璃瓶(850757C-1g)
5 mL透明玻璃密封安瓿(850757C-200mg)
5 mL透明玻璃密封安瓿(850757C-25mg)
5 mL透明玻璃密封安瓿(850757C-500mg)

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

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

靶器官

Central nervous system, Liver,Kidney

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

易制毒化学品(2类)
危险化学品

分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

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访问文档库

Mitochondria: Practical Protocols (2018)
Ionization Properties of Phospholipids Determined by Zeta Potential Measurements
Sathappa M and Alder NN
Bio-protocol, 6(22) (2016)
Charles G Cranfield et al.
Langmuir : the ACS journal of surfaces and colloids, 33(26), 6630-6637 (2017-06-14)
Cyclotides are cyclic disulfide-rich peptides that are chemically and thermally stable and possess pharmaceutical and insecticidal properties. The activities reported for cyclotides correlate with their ability to target phosphatidylethanolamine (PE)-phospholipids and disrupt cell membranes. However, the mechanism by which this
Sónia Troeira Henriques et al.
Journal of the American Chemical Society, 141(51), 20460-20469 (2019-11-26)
Peptides with pharmaceutical activities are attractive drug leads, and knowledge of their mode-of-action is essential for translation into the clinic. Comparison of native and enantiomeric peptides has long been used as a powerful approach to discriminate membrane- or receptor-mediated modes-of-action
Mariya Chavarha et al.
Langmuir : the ACS journal of surfaces and colloids, 28(48), 16596-16604 (2012-11-13)
Prior studies have shown that the biological mixture of the two hydrophobic surfactant proteins, SP-B and SP-C, produces faster adsorption of the surfactant lipids to an air/water interface, and that they induce 1-palmitoyl-2-oleoyl phosphatidylethanolamine (POPE) to form inverse bicontinuous cubic

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