Compound | Inhibition of Neutrophil Migration | Abnormal-CBD Receptor | GPR55 |
---|---|---|---|
Endogenous lipid mediators | |||
Virodhamine | +++ | ++a | ++b |
NADA | ++ | ++a | N.D. |
AEA | +++ | +a | ++b |
2-AG | 0 | 0a | ++b |
++c | |||
ARA-S | Antagonist | Agonistd | N.D. |
Antagoniste | |||
PEA | 0 | 0c | ++b |
LPI | 0 | N.D. | ++f,g |
Phytocannabinoids and related ligands | |||
(−)-CBD | +++ | +a ++c | ++b |
Partial agonist | Partial agonist | Antagonist | |
(+)-CBD | ++ | N.D. | N.D. |
Abnormal-CBD | ++ | ++c | ++h |
+a | +b | ||
O-1602 | ++ | +i | ++h |
++b | |||
Δ9-THC | 0 | 0a,c | ++b |
Other | |||
CP55940 | ++ | 0a | ++b |
SR141716A | Antagonist | Antagonista,c | Partial agonistj |
The symbols represent the potency or affinity of compounds being in the picomolar range (+++), nanomolar range (++), micromolar range (+), or not determined (N.D.).
↵ b Ryeberg et al. (2007).
↵ d Millman et al. (2005).
↵ e Zhang et al. (2006).
↵ g Oka et al. (2007) report that cannabinoid ligands do not activate GPR55.