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. 2021 Mar 24;22(7):3335. doi: 10.3390/ijms22073335

Figure 2.

Figure 2

Concentration-dependent vasopressin V1AR antagonist effect of (A) reference antagonist (d(CH2)51,Tyr(Me)2]-vasopressin (AVP)) and (B) active compounds from Cassia seeds (aurantio-obtusin and 2-hydroxyemodin 1-methylether). Reference drugs and test samples were tested at the indicated concentration for antagonist effect by determining the percentage inhibition of control response to 10 nM AVP. (B) Represents a comparative inhibition pattern of aurantio-obtusin with its substructure, 2-hydroxyemodin 1-methylether. Values are expressed as mean ± SD of triplicate experiment.