DEA

Discontinued Product

1485 has been discontinued.

View all CB<sub>1</sub> Receptors products.
说明: Endogenous CB1 agonist
别名: Docosatetraenylethanolamide
化学名: N-(2-Hydroxyethyl)-7Z,10Z,13Z,16Z-docosatetraenamide
说明书
引用文献
评论
文献 (2)

生物活性 for DEA

DEA is a potent endocannabinoid and anandamide (Cat. No. 1339) analog that activates CB1 receptors in microglia and binds to rat synaptosomal membranes (Ki = 34.4 nM). Cannabimimetic in vivo.

技术数据 for DEA

分子量 375.59
公式 C24H41NO2
储存 Desiccate at -20°C
CAS Number 150314-35-5
PubChem ID 5282273
InChI Key FMVHVRYFQIXOAF-DOFZRALJSA-N
Smiles CCCCC\C=C/C\C=C/C/C=C\C/C=C\CCCCCC(NCCO)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

参考文献 for DEA

参考文献是支持产品生物活性的出版物。

Barg et al (1995) Cannabinomimetic behavioral effects of and adenylate cyclase inhibition by two new endogenous anandamides. Eur.J.Pharmacol. 287 145 PMID: 8749028

Hanus et al (1993) Two new unsaturated fatty acid ethanolamides in brain that bind to the cannabinoid receptor. J.Med.Chem. 36 3032 PMID: 8411021

Walter et al (2001) Microglial cells produce endocannabinoids and express functional cannabinoid receptors: evidence that docosatetraenylethanolamide (DEA) is an additional endocannabinoid. Soc.Neurosci.Abstr. 634.16

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关键词: DEA, DEA supplier, Endogenous, CB1, agonists, Cannabinoids, Receptors, cb1r, Docosatetraenylethanolamide, 1485, Tocris Bioscience

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