Pricing Availability Delivery Time Qty
Cat.No. 1814 - N-ArachidonylGABA | C24H39NO3 | CAS No. 128201-89-8
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)

Biological Activity

Arachidonyl amino acid; first isolated from bovine brain. Inhibits pain in vivo.

Technical Data

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.

All Tocris products are intended for laboratory research use only.

Solubility Data

Solubility Soluble in ethanol (supplied pre-dissolved in anhydrous ethanol, 5mg/ml)

Preparing Stock Solutions

The following data is based on the product molecular weight 389.58. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 2.57 mL 12.83 mL 25.67 mL
5 mM 0.51 mL 2.57 mL 5.13 mL
10 mM 0.26 mL 1.28 mL 2.57 mL
50 mM 0.05 mL 0.26 mL 0.51 mL

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.


Dilution Calculator

Calculate the dilution required to prepare a stock solution.

Product Datasheets

Safety Datasheet


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

If you know of a relevant reference for N-ArachidonylGABA, please let us know.

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. Do you know of a great paper that uses N-ArachidonylGABA from Tocris? Please let us know.

Reviews for N-ArachidonylGABA

There are currently no reviews for this product. Be the first to review N-ArachidonylGABA and earn rewards!

Have you used N-ArachidonylGABA?

Submit a review and receive an Amazon gift card.

$50/€35/£30/$50CAN/¥300 Yuan/¥5000 Yen for first to review with an image

$25/€18/£15/$25CAN/¥75 Yuan/¥1250 Yen for a review with an image

$10/€7/£6/$10 CAD/¥70 Yuan/¥1110 Yen for a review without an image

Submit a Review

Literature in this Area

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

*Please note that Tocris will only send literature to established scientific business / institute addresses.

GABA Receptors

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.