ACPA (Arachidonylcyclopropylamide) - Moligand™, ≥98% , Agonist of CB 1 receptor;Agonist of GPR18, CAS No.229021-64-1, Agonist of CB 1 receptor;Agonist of GPR18
ACPA (Arachidonylcyclopropylamide) - Moligand™, ≥98% , Agonist of CB 1 receptor;Agonist of GPR18, CAS No.229021-64-1, Agonist of CB 1 receptor;Agonist of GPR18
GRADE & PURITYMoligand™?Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools.≥98%
Synonyms
acpa | GTPL739 | arachidonylcyclopropylamide | HMS3649N09 | Q4783530 | N-(Cyclopropyl)-5Z,8Z,11Z,14Z-eicosatetraenamide | NCGC00162405-01 | SCHEMBL6517985 | arachidonyl cyclopropylamide | SR-01000946681-1 | BA17967 | ACPA (in Tocrisolvetrade mark 100) | S
Potent, selective CB 1 agonist (K i = 2.2 nM), >300-fold selective over CB 2 receptors. Active in vivo .
Condiciones de almacenamiento de almacenamiento
Store at -20°C, Desiccated
Enviado en
Ice chest + Ice pads
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Grado
Moligand™
Tipo de acción
AGONIST
Mecanismo de acción
Agonist of CB 1 receptor;Agonist of GPR18
Nota
Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 6 months. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
This compound belongs to the class of organic compounds known as n-acyl amines. These are compounds containing a fatty acid moiety linked to an amine group through an ester linkage.
External Descriptors
Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
1.Xuexue Feng, Tielei Wu, Bingqing Yu, Yan Wang, Shian Zhong. (2017) Hydrophilic surface molecularly imprinted naringin prepared via reverse atom transfer radical polymerization with excellent recognition ability in a pure aqueous phase. RSC Advances, 7 (45):(28082-28091). [PMID:][10.1039/C7RA00202E]
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