For research use only. Not for therapeutic Use.
(±)-<wbr></wbr>CP 55,940 was one of the first bicyclic mimetics of Δ The racemic mixture of CP 55,940 is 20-<wbr></wbr> to 100-<wbr></wbr>fold more effective than Δ CP 55,940 has also been used to identify and characterize the central cannabinoid (CB<sub>1</sub>) receptor in rat brain membranes. The capacity to displace CP 55,940 from CB<sub>1</sub> receptor in rat brain preparations has frequently been used in the characterization of novel cannabimimetics.
Catalog Number | R064385 |
CAS Number | 83003-12-7 |
Synonyms | rel-5-(1,1-dimethylheptyl)-2-[(1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]-phenol |
Molecular Formula | C24H40O3 |
Purity | ≥95% |
Storage | -20°C |
IUPAC Name | 2-[(1R,2R,5R)-5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]-5-(2-methyloctan-2-yl)phenol |
InChI | InChI=1S/C24H40O3/c1-4-5-6-7-14-24(2,3)19-11-13-21(23(27)16-19)22-17-20(26)12-10-18(22)9-8-15-25/h11,13,16,18,20,22,25-27H,4-10,12,14-15,17H2,1-3H3/t18-,20-,22-/m1/s1 |
InChIKey | YNZFFALZMRAPHQ-SYYKKAFVSA-N |
SMILES | CCCCCCC(C)(C)C1=CC(=C(C=C1)C2CC(CCC2CCCO)O)O |
Reference | 1.Howlett, A.C.,Johnson, M.R.,Melvin, L.S., et al. Nonclassical cannabinoid analgetics inhibit adenylate cyclase: Development of a cannabinoid receptor model. Molecular Pharmacology 33, 297-302 (1987). |