Potentiation of .sup.3 H 2-(2-benzofuranyl)-2-imidazoline (BFI) binding sites in human tissue by tranylcypromine (TCP)

摘要

The present invention relates to a process for discovering compounds that modulate novel I.sub.2 binding sites (e.g. BFI binding sites) in human tissue, as well as a process for identifying TCP-like compounds that potentiate BFI binding.