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959761-62-7

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959761-62-7 Structure

959761-62-7 Structure
IdentificationBack Directory
[Name]

N-Arachidonoyl-3-hydroxy-γ-Aminobutyric Acid
[CAS]

959761-62-7
[Synonyms]

IBFIBMHGNMSQLB-DOFZRALJSA-N
N-Arachidonoyl-3-hydroxy-γ-Aminobutyric Acid
[Molecular Formula]

C24H39NO4
[MDL Number]

MFCD08062221
[MOL File]

959761-62-7.mol
[Molecular Weight]

405.57
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMF: 20 mg/ml; DMSO: 15 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 1 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS07
[Signal word ]

Danger
[Hazard statements ]

H225-H319-H336
[Precautionary statements ]

P210-P240-P241-P242-P243-P261-P264-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P312-P337+P313-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

Several different arachidonoyl amino acids, including N-arachidonoyl-3-hydroxy-γ-aminobutyric acid (NAG-3H-ABA), have been isolated and characterized from bovine brain.1 The glycine congener (NAGly; ) was further characterized and found to suppress formalin-induced pain in rats. NAG-3H-ABA was also found in rat brain by LC-MS techniques, but has not been fully characterized to date. Most arachidonoyl amino acids are poor ligands for the CB1 receptor.
[Definition]

ChEBI: N-arachidonoyl-3-hydroxy-gamma-aminobutyric acid is an organooxygen compound and an organonitrogen compound. It is functionally related to a gamma-amino acid.
[storage]

Store at -20°C
[References]

1. Huang, S.M., Bisogno, T., Petros, T.J., et al. Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain J. Biol. Chem. 276(46),42639-42644(2001).
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