Title of article :
Synthesis and biological evaluation of 14-alkoxymorphinans. 14.1 14-ethoxy-5-methyl substituted indolomorphinans with δ opioid receptor selectivity
Author/Authors :
Helmut Schmidhammer، نويسنده , , Dietmar Daurer، نويسنده , , Martina Wieser، نويسنده , , Krisztina Monory and، نويسنده , , Anna Borsodi، نويسنده , , Jackie Elliott and، نويسنده , , John R. Traynor، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 1997
Pages :
6
From page :
151
To page :
156
Abstract :
The 5-methyl and 14-ethoxy substituted analogues (compounds 2 – 4) of the δ opioid receptor antagonist naltrindole showed similar selectivity when compared with the reference drug. Compound 2 was a δ receptor antagonist in the mouse vas deferens preparation (MVD) exhibiting considerably higher selectivity ratios than naltrindole, while compound 4 was found to be a full and potent δ receptor agonist in the MVD.
Journal title :
Bioorganic & Medicinal Chemistry Letters
Serial Year :
1997
Journal title :
Bioorganic & Medicinal Chemistry Letters
Record number :
788528
Link To Document :
بازگشت