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| | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid Basic information |
| Product Name: | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid | | Synonyms: | N-ARACHIDONOYL-GAMMA-AMINOBUTYRIC ACID;N-ARACHIDONYLGABA;4-[(1-OXO-5Z,8Z,11Z,14Z-EICOSATETRAENYL)AMINO]-BUTANOIC ACID;N-ArachidonoylGABA;N-Arachidonoyl-γ-Aminobutyric Acid;N-Arachidonoyl-GABA (NA-GABA);Butanoic acid, 4-[[(5Z,8Z,11Z,14Z)-1-oxo-5,8,11,14-eicosatetraen-1-yl]amino]-;NArachidonylGABA,N ArachidonylGABA | | CAS: | 128201-89-8 | | MF: | C24H39NO3 | | MW: | 389.57 | | EINECS: | | | Product Categories: | Cannabinoid receptor | | Mol File: | 128201-89-8.mol | ![4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid Structure](CAS/GIF/128201-89-8.gif) |
| | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid Chemical Properties |
| Fp | 17°(63°F) | | storage temp. | Desiccate at -20°C | | solubility | DMF: 20 mg/ml; DMSO: 20 mg/ml; Ethanol: 50 mg/ml; PBS (pH 7.2): 2 mg/ml | | form | Pale yellow viscous oil. | | color | Colorless to light yellow | | Sensitive | Air Sensitive |
| | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid Usage And Synthesis |
| Uses | N-Arachidonoyl-GABA is one member of a new class of lipoamino acids related to anandamide identified in bovine brain. N-Arachidonoyl-GABA displays analgesic activity[1]. | | Definition | ChEBI: N-arachidonoyl-gamma-aminobutyric acid is an N-acyl-gamma-aminobutyric acid resulting from the formal condensation of the amino group of gamma-aminobutyric acid with the carboxy group of arachidonic acid. It has a role as a mammalian metabolite. It is a fatty amide and a N-acyl-gamma-aminobutyric acid. It is functionally related to an arachidonic acid. It is a conjugate acid of a N-arachidonoyl-gamma-aminobutyrate. | | Biological Activity | Arachidonyl amino acid; first isolated from bovine brain. Inhibits pain in vivo . | | storage | -20°C (desiccate) | | References | [1] Huang SM, et al. Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain. J Biol Chem. 2001 Nov 16;276(46):42639-44. DOI:10.1074/jbc.M107351200 |
| | 4-[[(5Z,8Z,11Z,14Z)-1-Oxo-5,8,11,14-eicosatetraenyl]amino]butanoic acid Preparation Products And Raw materials |
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