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. 2021 Dec 7;11:23528. doi: 10.1038/s41598-021-02843-6

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).