Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Arachidonoyl 2-chloroethylamide (ACEA) is a potent and selective cannabinoid (CB) receptor 1 agonist with Ki values of 1.4 and >2,000 nM for CB1 and CB2 receptors, respectively. In whole animal experiments, ACEA induces hypothermia in mice with the same efficacy as arachidonoyl ethanolamide , in spite of its higher affinity for the CB1 receptor. These data have been interpreted to indicate that ACEA may be a substrate for fatty acid amide hydrolase (FAAH), and thus only transiently available in whole animal experiments.
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
5 mg | 約 35 days | ¥ 22,500 |
10 mg | 約 35 days | ¥ 41,500 |
25 mg | 約 35 days | ¥ 95,500 |
50 mg | 約 35 days | ¥ 167,500 |
説明 | Arachidonoyl 2-chloroethylamide (ACEA) is a potent and selective cannabinoid (CB) receptor 1 agonist with Ki values of 1.4 and >2,000 nM for CB1 and CB2 receptors, respectively. In whole animal experiments, ACEA induces hypothermia in mice with the same efficacy as arachidonoyl ethanolamide , in spite of its higher affinity for the CB1 receptor. These data have been interpreted to indicate that ACEA may be a substrate for fatty acid amide hydrolase (FAAH), and thus only transiently available in whole animal experiments. |
別名 | 2'-chloro-AEA, Arachidonoyl 2'-Chloroethylamide |
分子量 | 365.98 |
分子式 | C22H36ClNO |
CAS No. | 220556-69-4 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 20 mg/mL
Ethanol: 25 mg/mL
DMF: 30 mg/mL
You can also refer to dose conversion for different animals. 詳細
bottom
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
ACEA 220556-69-4 Arachidonoyl 2'Chloroethylamide 2'-chloro-AEA Arachidonoyl 2'-Chloroethylamide Arachidonoyl 2' Chloroethylamide Inhibitor inhibitor inhibit