| Company Name: |
ChemeGen(Shanghai) Biotechnology Co.,Ltd. Gold
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| Tel: |
18818260767 |
| Email: |
sales@chemegen.com |
| Products Intro: |
Product Name:Arachidonoyl 2'-Chloroethylamide
CAS:220556-69-4
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
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- ACEA
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- $142.00
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2026-07-15
- CAS:220556-69-4
- Purity:
- Supply Ability: 10g
- ACEA
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2026-07-13
- CAS:220556-69-4
- Min. Order: 1KG
- Purity: 98%
- Supply Ability: 1000kg
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| RTECS | JX3840800 | | storage temp. | −20°C | | solubility | DMSO: soluble | | form | oil | | color | pale yellow | | Sensitive | Air Sensitive | | InChIKey | SCJNCDSAIRBRIA-DOFZRALJSA-N | | SMILES | C(NCCCl)(=O)CCC/C=C\C/C=C\C/C=C\C/C=C\CCCCC |
| Description | 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 (AEA; ), 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. | | Uses | A synthetic agonist of the cannabinoid receptor 1 (CB1R). ACEA is considered to be a selective cannabinoid agonist as it binds primarily to the CB1R and has low affinity to the cannabinoid receptor 2
(CB2R). | | Definition | ChEBI: Arachidonyl-2'-chloroethylamide is a fatty amide obtained by the formal condensation of arachidonic acid with 2-chloroethanamine. It is a potent agonist of the CB1 receptor (Ki = 1.4 nM) and also has a low affinity for the CB2 receptor (Ki = 3100 nM). It has a role as a CB1 receptor agonist, a neuroprotective agent and a CB2 receptor agonist. It is an organochlorine compound, a secondary carboxamide, a fatty amide and a synthetic cannabinoid. It is functionally related to an arachidonic acid. | | Biological Activity | Potent and highly selective CB 1 receptor agonist (K i = 1.4 nM). Displays > 1400-fold selectivity over CB 2 receptors. Active in vivo . Also available as part of the Cannabinoid CB 1 Receptor Tocriset™ . | | Biochem/physiol Actions | Potent and selective neuronal CB1 cannabinoid receptor agonist. | | Enzyme inhibitor | This synthetic CB1 receptor agonist and anandamide (N- arachidonylethanolamide) analogue (FW = 365.99 g/mol; CAS 220556-69-4; Symbol: ACEA) is a selective agonist of cannabinoid receptor-1 (Ki = 1.4 nM) but has low affinity to the cannabinoid receptor 2 (Ki = 3.1 μM). ACEA inhibits forskolin-induced cAMP accumulation in Chinese hamster ovary cells expressing the human CB1 receptor. It also increases the binding of [ 35 S]GTPgS to cerebellar membranes and inhibits electrically evoked contractions of the mouse vas deferens. ACEA produces hypothermia in mice, an effect that is inhibited by co-administration of the CB1 receptor antagonist SR141716A. | | storage | Store at -20°C |
| | ACEA Preparation Products And Raw materials |
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