“…Structurally related isoquinoline derivatives, such as annonaine, nornuciferine, and asimilobine, isolated from the fruit of Annona muricata, have been shown to inhibit the binding of [ 3 H]rauwolscine to 5-HT 1A receptors in calf hippocampus (Figure 4). The IC 50 values for inhibition of receptor binding for annonaine, nornuciferine, and asimilobine were 3, 9, and 5 M, respectively (Hasrat et al, 1997b), which are close to the K i values of O-methyldauricine (1) (4.5 M) and popisidine (2) (5.8 M). In the functional assay, based on the inhibition of the accumulation of cAMP in NIH-3T3 cells stably transfected with 5-HT 1A receptor from human, the K i values for annonaine, nornuciferine, and asimilobine were estimated to be less than 10 M (Hasrat et al, 1997a).…”