Discontinued Product

N-ArachidonylGABA (Cat. No. 1814) has been withdrawn from sale for commercial reasons.
Description: Inhibits pain in vivo
Alternative Names: NAGABA
Chemical Name: 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid
Purity: ≥98% (HPLC)
Literature (1)

Biological Activity for N-ArachidonylGABA

N-ArachidonylGABA is an arachidonyl amino acid; first isolated from bovine brain. Inhibits pain in vivo.

Technical Data for N-ArachidonylGABA

M. Wt 389.58
Formula C24H39NO3
Storage Desiccate at -20°C
Purity ≥98% (HPLC)
CAS Number 128201-89-8
PubChem ID 16759310

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.

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

Product Datasheets for N-ArachidonylGABA

References for N-ArachidonylGABA

References are publications that support the biological activity of the product.

El Fangour et al (2003) Hemisynthesis and preliminary evaluation of novel endocannabinoid analogues. Bioorg.Med.Chem.Lett. 13 1977 PMID: 12781177

Huang et al (2001) Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain. J.Biol.Chem. 276 42639 PMID: 11518719

Keywords: N-ArachidonylGABA, N-ArachidonylGABA supplier, inhibitors, inhibits, pain, vivo, cannabinoids, Receptors, GABAB, GABA, GABAA, GABAC, NAGABA, Miscellaneous, Other, Cannabinoids, 1814, Tocris Bioscience

Citations for N-ArachidonylGABA

Citations are publications that use Tocris products.

Currently there are no citations for N-ArachidonylGABA.

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Literature in this Area

Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!

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GABA Receptors Scientific Review

GABA Receptors Scientific Review

Written by Ian Martin, Norman Bowery and Susan Dunn, this review provides a history of the GABA receptor, as well as discussing the structure and function of the various subtypes and the clinical potential of receptor modulators; compounds available from Tocris are listed.