The discovery of a novel series of 8-azabicyclo[3.2.1]octan-3-yl)-3-(4-chlorophenyl) propanamide antagonists of the vasopressin V(1A) receptor is disclosed. Compounds 47 and 48 were found to be high affinity, selective vasopressin V(1A) antagonists.
Journal article
2011-05-15T00:00:00+00:00
21
3163 - 3167
4
Amides, Antidiuretic Hormone Receptor Antagonists, Aza Compounds, Cells, Cultured, Cyclization, Drug Discovery, Humans, Liver, Molecular Structure, Protein Binding