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Merck
CN

850757C

Avanti

磷脂酰乙醇胺(16:0-18:1 PE)

Avanti Research™ - A Croda Brand

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

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关于此项目

经验公式（希尔记法）:
C39H76NO8P
化学文摘社编号:
26662-94-2
分子量:
718.00
MDL number:
MFCD00672608
UNSPSC Code:
51191904
NACRES:
NA.25

主要文件

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产品名称

磷脂酰乙醇胺(16:0-18:1 PE), Avanti Research™ - A Croda Brand

SMILES string

[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

description

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

assay

>99% (TLC)

form

liquid

packaging

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)

manufacturer/tradename

Avanti Research™ - A Croda Brand

concentration

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

lipid type

cardiolipins
phospholipids

shipped in

dry ice

storage temp.

−20°C

相关类别

Application

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。

Packaging

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)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system, Liver,Kidney

存储类别

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

易制毒化学品（2类）
危险化学品
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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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Ionization Properties of Phospholipids Determined by Zeta Potential Measurements
Sathappa M and Alder NN
Bio-protocol, 6(22) (2016)
Mitochondria: Practical Protocols (2018)
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
Tânia Silva et al.
Langmuir : the ACS journal of surfaces and colloids, 34(5), 2158-2170 (2018-01-07)
An understanding of the mechanism of action of antimicrobial peptides is fundamental to the development of new and more active antibiotics. In the present work, we use a wide range of techniques (SANS, SAXD, DSC, ITC, CD, and confocal and
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
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