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Merck
CN

840034C

Avanti

16:0-18:1 PS (POPS)

Avanti Research™ - A Croda Brand

别名:

1-十六烷酰基-2-(9Z-十八烯酰基)-sn-甘油-3-磷酸-L-丝氨酸（钠盐）；POPS; PS(16:0/18:1(9Z)); 110669

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关于此项目

经验公式（希尔记法）:
C40H75NO10PNa
CAS Number:
321863-21-2
分子量:
783.99
MDL编号:
MFCD00674276
UNSPSC代码:
12352211
NACRES:
NA.25

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描述

1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-L-serine (sodium salt), chloroform

方案

>99% (TLC)

表单

liquid

包装

pkg of 1 × 1 mL (840034C-10mg)
pkg of 1 × 2.5 mL (840034C-25mg)
pkg of 2 × 4 mL (840034C-200mg)
pkg of 5 × 4 mL (840034C-500mg)

制造商/商品名称

Avanti Research™ - A Croda Brand

浓度

10 mg/mL (840034C-10mg)
10 mg/mL (840034C-25mg)
25 mg/mL (840034C-200mg)
25 mg/mL (840034C-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-])(OC[C@](C([O-])=O)([H])[NH3+])=O)(OC(CCCCCCC/C=C\CCCCCCCC)=O)COC(CCCCCCCCCCCCCCC)=O.[Na+]

InChI key

RQYKXRYGZHMUSU-JEAFVVATSA-M

相关类别

包装

5 mL透明玻璃密封安瓿（840034C-10mg）
5 mL透明玻璃密封安瓿（840034C-200mg）
5 mL透明玻璃密封安瓿（840034C-25mg）
5 mL透明玻璃密封安瓿（840034C-500mg）

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形图

Skull and crossbonesHealth hazard
GHS06,GHS08

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

储存分类代码

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

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

危险化学品
易制毒化学品（2类）

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Carina Drechsler et al.
Biophysical journal, 115(8), 1509-1517 (2018-09-30)
Lipid asymmetries between the outer and inner leaflet of the lipid bilayer exist in nearly all biological membranes. Although living cells spend great effort to adjust and maintain these asymmetries, little is known about the biophysical phenomena within asymmetric membranes
Li-Ping Gao et al.
Biochimica et biophysica acta. General subjects, 1864(1), 129422-129422 (2019-09-07)
Previous studies suggested that fibrillar human IAPP (hIAPP) is more likely to deposit in β-cells, resulting in β-cell injury. However, the changes in the conformation of hIAPP in lipid environment and the mechanism involved in β-cell damage are unclear. Synthetic
Kari Kusler et al.
The journal of physical chemistry. B, 120(50), 12883-12889 (2016-12-14)
Phosphatidylserine (PS) has previously been found to bind Cu2+ in a ratio of 1 Cu2+ ion per 2 PS lipids to form a complex with an apparent dissociation constant that can be as low as picomolar. While the affinity of
Josef Melcr et al.
Journal of chemical theory and computation, 16(1), 738-748 (2019-11-26)
Phosphatidylserine (PS) lipids are important signaling molecules and the most common negatively charged lipids in eukaryotic membranes. The signaling can be often regulated by calcium, but its interactions with PS headgroups are not fully understood. Classical molecular dynamics (MD) simulations
Irene S Tobias et al.
The Biochemical journal, 473(4), 509-523 (2015-12-05)
Atypical protein kinase C (aPKC) isoenzymes are key modulators of insulin signalling, and their dysfunction correlates with insulin-resistant states in both mice and humans. Despite the engaged interest in the importance of aPKCs to type 2 diabetes, much less is
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