Author/Authors :
Helmut Schmidhammer، نويسنده , , Angelika Stangl، نويسنده , , Zsuzsanna Fürst، نويسنده , , Eva Szabo، نويسنده , , Anna Borsodi، نويسنده , , Dinesh Patel and، نويسنده , , John R. Traynor، نويسنده ,
Abstract :
The N-phenethyl analogue (compound 4) of the μ-selective opioid antagonist cyprodime (1) has been prepared and evaluated in radioligand binding, bioassays (guinea-pig ileum myenteric plexus and mouse vas deferens preparations) and the rat tail flick test. It was found to possess remarkable affinity and high preference for μ opioid receptors and high antinociceptive potency which is comparable to its N-methyl analogue 3.