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Arachidonoyl amide
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Arachidonoyl amide图片
CAS NO:85146-53-8
包装与价格:
包装价格(元)
10mg (solution)电议
25mg (solution)电议
50mg (solution)电议

产品介绍

化学性质

Physical AppearanceA solution in acetate. To change the solvent, simply evaporate the acetate containing under a gentle stream of nitrogen and immediately add the solvent of choice.
StorageStore at -20°C
M.Wt303.5
Cas No.85146-53-8
FormulaC20H33NO
SynonymsArachidonamide,Arachidonic Acid amide
Solubility≤10mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in dimethyl formamide
Chemical Name5Z,8Z,11Z,14Z-eicosatetraenamide
Canonical SMILESCCCCC/C=C\C/C=C\C/C=C\C/C=C\CCCC(=O)N
运输条件蓝冰运输或根据您的需求运输。
一般建议为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

Arachidonoyl amide is a CB1 receptor agonist [1]. The cannabinoid receptor type 1, abbreviated as CB1, is a G protein-coupled cannabinoid receptor expressed primarily in the central and peripheral nervous system. CB1 receptor has been implicated in maintaining the homeostasis in health and disease. Overexpression of CB1 receptor has been found in human hepatocellular carcinoma tumor samples and other human prostate cancer cells [2].

Arachidonoyl amide is an analog of anandamide (AEA) that lacks the hydroxyethyl moiety. It was hydrolyzed by FAAH more effectively than AEA but exhibited significantly weaker binding to the human CB1 receptor with a Ki of 9.6 μM [1]. Arachidonoyl amide exhibited similar binding and translocation into cells via the AEA transporter compared to AEA. Arachidonoyl amide inhibited [3H]-AEA uptake into human astrocytoma cells with an IC50 of 9 μM [3].

References:
[1] Felder C C, Briley E M, Axelrod J, et al.  Anandamide, an endogenous cannabimimetic eicosanoid, binds to the cloned human cannabinoid receptor and stimulates receptor-mediated signal transduction[J]. Proceedings of the National Academy of Sciences, 1993, 90(16): 7656-7660.
[2] Pertwee R G.  The diverse CB1 and CB2 receptor pharmacology of three plant cannabinoids: Δ9‐ etrahydrocannabinol, cannabidiol and Δ9‐ etrahydrocannabivarin[J]. British journal of pharmacology, 2008, 153(2): 199-215.
[3] Piomelli, D. ,Beltramo, M.,Glasnapp, S., et al. Structural determinants for recognition and translocation by the anandamide transporter. Proceedings of the National Academy of Sciences of the United States of America 96, 5802-5807 (1999).