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Merck
CN

800715P

Avanti

N-P Serine PA

Avanti Research - A Croda Brand

别名:

N-palmitoyl-serine phosphoric acid (ammonium salt)

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关于此项目

经验公式(希尔记法):
C19H44N3O7P
化学文摘社编号:
分子量:
457.54
MDL编号:
UNSPSC代码:
12352211
NACRES:
NA.25
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产品名称

N-P Serine PA, Avanti Research - A Croda Brand 800715P, powder

方案

>99% (TLC)

表单

powder

包装

pkg of 1 × 1 mg (800715P-1mg)

制造商/商品名称

Avanti Research - A Croda Brand 800715P

脂质类型

phosphoglycerides

运输

dry ice

储存温度

−20°C

一般描述

Lysophosphatidic acid (LPA) receptor modulators include N-palmitoyl serine phosphoric acid and N-palmitoyl-tyrosine phosphoric acid. N-palmitoyl serine phosphoric acid is a competitive inhibitor of the LPA receptor in Xenopus oocytes. However, in mammalian cells, N-palmitoyl-serine phosphoric acid may act as an agonist for the LPA receptor. LPA is a lipid mediator that acts similar to growth factors through G-protein coupled plasma membrane receptors. LPA may play a role in platelet aggregation, smooth muscle contraction, vasoactive changes, cytoskeletal reorganization and cell proliferation. N-palmitoyl serine phosphoric acid may also play a role in signal transduction in mammalian cells by increasing intracellular calcium.
N-palmitoyl serine phosphoric acid prevents human platelet aggregation, which is induced by 1-hexadecyl-2-lyso-sn-glycero-3-phosphate.

包装

5 mL Amber Glass Screw Cap Vial (800715P-1mg)

制备说明

Product use: A range of 0.1-20 mM of N-palmitoyl serine phosphoric acid can be used for cell studies. Make a stock solution of 5 mM in DMSO and store at -20°C. Diluted N-palmitoyl serine phosphoric acid can be directly added to the study medium. An et al. dissolved N-palmitoyl-serine and N-palmitoyl-tyrosine phosphoric acid in 0.1 mL PBS containing 0.1 mg/mL human serum albumin before adding to cells. In X. laevis studies, these LPA inhibitors were dissolved in DMSO at 1 mM and filtered through a 0.45 mM membrane filter before injection.

法律信息

Avanti Research is a trademark of Avanti Polar Lipids, LLC

储存分类代码

11 - Combustible Solids

法规信息

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S B Hooks et al.
Molecular pharmacology, 53(2), 188-194 (1998-03-14)
Despite an intriguing cell biology and the suggestion of a role in pathophysiological responses, the mechanism of action of such lipid phosphoric acid mediators as lysophosphatidic acid (LPA) remains obscure, in part because of an underdeveloped medicinal chemistry. We report
Characterization of a receptor subtype-selective lysophosphatidic acid mimetic
Hooks, S.B, et. al.
Molecular Pharmacology, 53, 188-194 (1998)
Chung-Ren Jan et al.
Pharmacology & toxicology, 93(2), 71-76 (2003-08-06)
The effect of N-palmitoyl-L-serine phosphoric acid (L-NASPA), which has been used as an inhibitor of lysophosphatidic acid receptors, on intracellular Ca2+ concentration ([Ca2+]i) in human osteosarcoma MG63 cells was measured by using fura-2. L-NASPA (0.1-10 microM) caused a rapid and
Novel effect of N-palmitoyl-L-serine phosphoric acid on cytosolic Ca2+ levels in human osteoblasts
Jan, C.R
Pharmacology & Toxicology, 93, 71-76 (2003)
S An et al.
Molecular pharmacology, 54(5), 881-888 (1998-11-06)
Mobilization of intracellular Ca2+ is a critical cellular response to lysophosphatidic acid (LPA) in many cell types. Recent identification of endothelial differentiation gene (Edg) 2 and Edg4 as subtypes of G protein-coupled receptors for LPA allowed examination of the Ca2+

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