Table 1. Affinities of Leu-Enkephalin and Compounds 1–8 on DOPra.
The binding affinity (Ki) of each compound was determined by its ability to inhibit the binding of [3H]-deltorphin II (competitive binding), a selective DOPr agonist, to GH3/DOPr cell membrane extracts. Ki values are the means ± SEM of three separate experiments each performed in triplicate.