Table 3.
Human dopamine D1, D2, D3, and D4 and vasopressin V1A receptor binding data of isoliquiritigenin.
| Receptors | Radioligand | % Inhibition of control-specific bindinga | Reference antagonist | Reference IC50b |
|---|---|---|---|---|
| D1 | [3H]SCH23390 | 96.0 | SCH23390 | 0.5 |
| D2L | [3H]methylspiperone | 21.3 | (+)Butaclamol | 2.6 |
| D3 | [3H]methylspiperone | 52.2 | (+)Butaclamol | 4.1 |
| D4 | [3H]methylspiperone | 44.8 | Clozapine | 93 |
| V1A* | [3H]AVP | 60.8 | [d(CH2)51,Tyr(Me)2]-AVP | 1.4 |
*Agonist binding.
aValues are presented as the mean of the percent inhibition of control specific binding by 100 µM isoliquiritigenin performed in duplicate.
bThe IC50 value of the reference antagonist (nM).