870436P
Avanti
C16:0 anandamide phosphate
Avanti Research™ - A Croda Brand
别名:
palmitoyl ethanolamide phosphate (sodium salt)
产品名称
C16:0 anandamide phosphate, Avanti Research™ - A Croda Brand 870436P, powder
方案
>99% (TLC)
表单
powder
包装
pkg of 1 × 1 mg (870436P-1mg)
制造商/商品名称
Avanti Research™ - A Croda Brand 870436P
运输
dry ice
储存温度
−20°C
SMILES字符串
O=C(CCCCCCCCCCCCCCC)NCCOP(O)([O-])=O.[Na+]
一般描述
C16:0 anandamide is fatty acid amide, endogenic in nature. It is a member of the N-acylethanolamines family. Palmitoyl ethanolamide is present in egg yolk and peanut.
C16:0 anandamide phosphate is a phosphate ester of C16:0 anandamide. C16:0 anandamide, also known as N-palmitoyl ethanolamide, is a N-acyl ethanolamide derivative of palmitic acid.
生化/生理作用
Anandamide is a ligand for cannabinoid receptors. Anandamide possesses anti-inflammatory and pain killing action. It is effective in relieving pain associated with nerve compression syndrome and pudendal neuralgia. Anandamide is also useful in treating atopic eczema. Its effect is mediated by cannabinoid CB1 and CB2 receptors.
C16:0 anandamide or palmitoyl ethanolamide exhibits anti-inflammatory and analgesic properties. It is currently used as a veterinary anti-inflammatory agent.
包装
5 mL Amber Glass Screw Cap Vial (870436P-1mg)
法律信息
Avanti Research is a trademark of Avanti Polar Lipids, LLC
储存分类代码
11 - Combustible Solids
闪点(°F)
No data available
闪点(°C)
No data available
法规信息
新产品
此项目有
Palmitoylethanolamide ameliorates carbon tetrachloride-induced liver fibrosis in rats
Ohara M, et al.
Frontiers in Pharmacology, 9, 698-711 (2018)
Ocular hypotensive effect of oral palmitoyl-ethanolamide: a clinical trial
Gagliano C, et al.
Investigative Ophthalmology & Visual Science, 52(9), 6096-6100 (2011)
Protective role of palmitoylethanolamide in contact allergic dermatitis
Petrosino S, et al.
Allergy, 65(6), 698-711 (2010)
Daria Vinokurova et al.
Frontiers in pharmacology, 9, 698-698 (2018-07-19)
Epipial application is one of the approaches for drug delivery into the cortex. However, passive diffusion of epipially applied drugs through the cortical depth may be slow, and different drug concentrations may be achieved at different rates across the cortical
Anandamide receptors
Di Marzo V, et al.
Prostaglandins, Leukotrienes, and Essential Fatty Acids, 66(2-3), 377-391 (2002)
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