Product overview

Name N-ArachidonylGABA
Alternative names NAGABA
Purity >98%
Description Arachidonyl amino acid
Write Your Own Review
You're reviewing:N-ArachidonylGABA
Rate this item:

Biological Data

Biological description An endogenously produced arachidonyl amino acid. Thought to act through T-type calcium channels to show antinociceptive actions.

Solubility & Handling

Solubility overview Soluble in ethanol (5mg/ml)
Storage instructions -20°C (desiccate)
Storage of solutions Prepare and use solutions on the same day if possible. Store solutions at -20°C for up to one month if storage is required. Equilibrate to RT and ensure the solution is precipitate free before use.
Shipping Conditions Stable for ambient temperature shipping. Follow storage instructions on receipt.
Important This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use.

Calculators

Molarity

=
x
x
More Info

Dilution

x
=
x
More Info

Chemical Data

Purity >98%
Chemical name 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14 -eicosatetraenyl]amino]butanoic acid
Molecular Weight 389.58
Chemical structure N-ArachidonylGABA  [128201-89-8] Chemical Structure
Molecular Formula C24H39NO3
CAS Number 128201-89-8
PubChem identifier 16759310
SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCCCC(O)=O
InChiKey JKUDIEXTAYKJNX-DOFZRALJSA-N

References for N-ArachidonylGABA

References are publications that support the biological activity of the product
  • Quantitative LC-MS/MS analysis of arachidonoyl amino acids in mouse brain with treatment of FAAH inhibitor.

    Han B et al (2013) Anal Biochem 432(2) : 74-81.
  • T-type calcium channel inhibition underlies the analgesic effects of the endogenous lipoamino acids.

    Barbara G et al (2009) J Neurosci 29(42) : 13106-14.
  • Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain.

    Huang SM et al (2001) J Biol Chem 276(46) : 42639-44.

3 Item(s)