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Biological Data
| Biological description | An endogenously produced arachidonyl amino acid. Thought to act through T-type calcium channels to show antinociceptive actions. |
Solubility & Handling
| Storage instructions | -20°C (desiccate) |
| Solubility overview | Soluble in ethanol (5mg/ml) |
| Important | This product is for RESEARCH USE ONLY and is not intended for therapeutic or diagnostic use. Not for human or veterinary use. |
Chemical Data
| Chemical name | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14 -eicosatetraenyl]amino]butanoic acid |
| Chemical structure | ![N-ArachidonylGABA [128201-89-8] Chemical Structure](data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAAEAAAABCAQAAAC1HAwCAAAAC0lEQVR4nGP6zwAAAgcBApocMXEAAAAASUVORK5CYII= "N-ArachidonylGABA [128201-89-8]") |
| Molecular Formula | C24H39NO3 |
| 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
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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.
![N-ArachidonylGABA [128201-89-8] Chemical Structure](https://hellobio.com/media/catalog/product//h/b/hb0856.png "N-ArachidonylGABA [128201-89-8]")
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