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. Author manuscript; available in PMC: 2020 Jan 5.
Published in final edited form as: Eur J Pharmacol. 2018 Oct 25;842:351–364. doi: 10.1016/j.ejphar.2018.10.028

Fig. 2A-G. NET specificity of D22 analogs by displacement of [3H]Nisoxetine binding in mouse hippocampus.

Fig. 2A-G.

Compounds 1–7 (A-G, black, open circles) were tested for their ability to displace the high-affinity NET blocker [3H]nisoxetine in 120 min binding assays performed on ice. Concentration-response curves obtained for unlabeled reference compounds are repeated in gray for each subfigure and include NET substrate dopamine (gray, closed squares), inhibitor desipramine (gray, closed circle), and decynium-22 (D22, gray, open square). The IC50 determinations obtained from non-linear regression curve fits can be found in Table 2.