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Merck

870818M

Avanti

N-arachidonoylglycine

Avanti Research - A Croda Brand 870818M, methylene chloride solution

别名:

methylene chloride solution

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About This Item

经验公式(希尔记法):
C22H35NO3
分子量:
361.52
分類程式碼代碼:
12352211
NACRES:
NA.25

形狀

methylene chloride solution

包裝

pkg of 1 × 1 mL (870818M-10mg)

製造商/商標名

Avanti Research - A Croda Brand 870818M

脂質類型

neutral glycerides
neutral lipids

運輸包裝

dry ice

儲存溫度

−20°C

SMILES 字串

O=C(CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC)NCC(O)=O

InChI

1S/C22H35NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-21(24)23-20-22(25)26/h6-7,9-10,12-13,15-16H,2-5,8,11,14,17-20H2,1H3,(H,23,24)(H,25,26)/b7-6-,10-9-,13-12-,16-15-

InChI 密鑰

YLEARPUNMCCKMP-DOFZRALJSA-N

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一般說明

N-arachidonoylglycine (NAgly) is an endogenous ligand and a signaling lipid. It belongs to the eicosanoid family. NAgly is a natural ligand to activate G-protein coupled receptor, namely GPR18. It is found in rat brain and spinal cord.

生化/生理作用

N-arachidonoylglycine (NAgly) exhibits analgesic effects.

包裝

2 mL Amber Glass Sealed Ampule (870818M-10mg)

法律資訊

Avanti Research is a trademark of Avanti Polar Lipids, LLC

象形圖

Health hazardExclamation mark

訊號詞

Warning

危險分類

Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Central nervous system

水污染物質分類(WGK)

WGK 2


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Resolution of inflammation by N-arachidonoylglycine
Burstein S H, et al.
Journal of Cellular Biochemistry, 112(11), 3227-3233 (2011)
S M Huang et al.
The Journal of biological chemistry, 276(46), 42639-42644 (2001-08-24)
In mammals, specific lipids and amino acids serve as crucial signaling molecules. In bacteria, conjugates of lipids and amino acids (referred to as lipoamino acids) have been identified and found to possess biological activity. Here, we report that mammals also
T Sheskin et al.
Journal of medicinal chemistry, 40(5), 659-667 (1997-02-28)
In order to establish the structural requirements for binding to the brain cannabinoid receptor (CB1), we have synthesized numerous fatty acid amides, ethanolamides, and some related simple derivatives and have determined their Ki values. A few alpha-methyl- or alpha, alpha-dimethylarachidonoylalkylamides
S H Burstein et al.
Prostaglandins & other lipid mediators, 61(1-2), 29-41 (2000-04-29)
In addition to the well studied hydrolytic metabolism of anandamide, a number of oxidative processes are also possible. Several routes somewhat analogous to the metabolism of free arachidonic acid have been reported. These involve mediation by various lipoxygenases and COX-2
Identification of N-arachidonylglycine as the endogenous ligand for orphan G-protein-coupled receptor GPR18
Kohno M, et al.
Biochemical and Biophysical Research Communications, 347(3), 827-832 (2006)

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