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Merck
CN

857230P

Avanti

C18:1 LPA

Avanti Research - A Croda Brand

别名:

1-O-9-(Z)-十八烯基-sn-甘油-3-磷酸酯(铵盐); PA(18:1(9Z)e/0:0)

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关于此项目

经验公式(希尔记法):
C21H46NO6P
化学文摘社编号:
分子量:
439.57
UNSPSC代码:
51191904
NACRES:
NA.25
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产品名称

C18:1 LPA, 1-(9Z-octadecenyl)-2-hydroxy-sn-glycero-3-phosphate (ammonium salt), powder

方案

>99% (LPA; may contain up to 10% of the 2-LPA isomer, TLC)

表单

powder

包装

pkg of 1 × 1 mg (857230P-1mg)

制造商/商品名称

Avanti Research - A Croda Brand 857230P

脂质类型

cardiolipins
phospholipids

运输

dry ice

储存温度

−20°C

SMILES字符串

O[C@](COP([O-])(O)=O)([H])COCCCCCCCC/C=C\CCCCCCCC.[NH4+]

InChI key

WEOSAIXAEGBVPQ-WBIWQBECSA-N

一般描述

C18:1 LPA是一种生物活性脂质。该溶血磷脂酸(LPA)是从膜磷脂中获得的可溶性脂质。它存在于血浆中。

应用

C18:1 LPA适合在萤光素酶测定中刺激人胚胎肾293(HEK 293)细胞。它还适合作为达尔伯克氏改良伊格尔培养基(DMEM)的添加剂,用于跨孔迁移试验、伤口愈合试验和细胞增殖试验。′

生化/生理作用

溶血磷脂酸(LPA)信号转导参与多种细胞过程。它还与神经系统疾病、炎症和癌症有关。

包装

5 mL透明玻璃密封安瓿(857230P-1mg)

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

No data available

闪点(°C)

No data available


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Autotaxin is a novel target of micro RNA-101-3p
Wang Y, et al.
FEBS Open Bio, 9(4), 707- 716 (2019)
Lysophosphatidic acid and its receptor LPA1 mediate carrageenan induced inflammatory pain in mice
Srikanth M, et al.
European Journal of Pharmacology, 841, 49- 56 (2018)
R D Moreno-Fernández et al.
Neuropharmacology, 164, 107896-107896 (2019-12-08)
The LPA1 receptor, one of the six characterized G protein-coupled receptors (LPA1-6) through which lysophosphatidic acid acts, is likely involved in promoting normal emotional behaviours. Current data suggest that the LPA-LPA1-receptor pathway may be involved in mediating the negative consequences
Jesica R Williams et al.
The Journal of biological chemistry, 284(25), 17304-17319 (2009-04-16)
Lysophosphatidic acid (LPA) is a ligand for LPA(1-3) of the endothelial differentiation gene family G-protein-coupled receptors, and LPA(4-8) is related to the purinergic family G-protein-coupled receptor. Because the structure-activity relationship (SAR) of GPR92/LPA(5) is limited and whether LPA is its

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