For research use only. Not for therapeutic Use.
A regioisomer of cannabidiol without psychotropic activity; inactive at CB1 or CB2 receptors. However, it activates a third type of non-CB1/CB2 endo-cannabinoid receptor. Mechanism is under study
| Catalog Number | R028062 |
| CAS Number | 22972-55-0 |
| Molecular Formula | C21H30O2 |
| Purity | ≥95% |
| IUPAC Name | 4-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-5-pentylbenzene-1,3-diol |
| InChI | InChI=1S/C21H30O2/c1-5-6-7-8-16-12-17(22)13-20(23)21(16)19-11-15(4)9-10-18(19)14(2)3/h11-13,18-19,22-23H,2,5-10H2,1,3-4H3/t18-,19+/m0/s1 |
| SMILES | CCCCCC1=C(C(=CC(=C1)O)O)[C@@H]2C=C(CC[C@H]2C(=C)C)C |
| Reference | Z Járai et al. Cannabinoid-induced mesenteric vasodilation through an endothelial site distinct from CB1 or CB2 receptors. Proc. Natl. Acad. Sci. USA 1999, 96(24), 14136-14141.
L Walter et al. Nonpsychotropic cannabinoid receptors regulate microglial cell migration. J. Neurosci. 2003, 23(4), 1398-1405. |
