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- 规格参数
- 包装参数
Biochem/physiol Actions
An analog of arachidonylethanolamide (anandamide) that is a potent, selective CB1 cannabinoid receptor agonist. The methyl group at the C-2 position of arachidonic acid gives the compound enhanced metabolic stability. It can fully substitute for Δ9-THC in animal self-administration tests.
Anandamide analog; potent, selective CB1 cannabinoid receptor agonist.
Disclaimer
Supply conditions do not apply to the regions and states of Brazil: North, Northeast, Mato Grosso do Sul, Mato Grosso, and Rio Grande do Sul.
| Quality Segment | 200 |
| assay | ≥95% |
| form | ethanol solution |
| drug control | regulated under CDSA - not available from Sigma-Aldrich Canada |
| shipped in | wet ice |
| storage temp. | −20°C |
| SMILES string | CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCC(C)C(=O)NCCF |
| InChI | 1S/C23H38FNO/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-22(2)23(26)25-21-20-24/h7-8,10-11,13-14,16-17,22H,3-6,9,12,15,18-21H2,1-2H3,(H,25,26)/b8-7-,11-10-,14-13-,17-16- |
| InChI key | HMMNZALKMVCHHZ-ZKWNWVNESA-N |
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