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. 2018 Sep 20;8:14087. doi: 10.1038/s41598-018-32568-y

Table 1.

Affinity values (Ki) for the binding to human κ-, rat μ, or rat δ-opioid receptors.

Compounds µ binding affinity Ki (nM) δ binding affinity Ki (nM) κ binding affinity Ki (nM)
Dezocine 1.46 ± 0.10 398.6 ± 43.25 22.01 ± 1.52
DAMGO 2.30 ± 0.02
DPDPE 4.36 ± 0.69
U50,488 H, 0.91 ± 0.20

Membranes were incubated with varying concentrations of ligands in the presence of 2.0 nM [3H]DAMGO, 1.1 nM [3H]DPDPE and 1.5 nM [3H]U69593. Data are expressed as the mean ± SEM for at least three independent experiments performed in triplicate.