The discovery of novel 8-azabicyclo[3.2.1]octan-3-yl)-3-(4-chlorophenyl) propanamides as vasopressin V1A receptor antagonists.

Napier S., Wishart G., Arbuckle W., Baker J., Barn D., Bingham M., Brown A., Byford A., Claxton C., Craighead M., Buchanan K., Fielding L., Gibson L., Goodwin R., Goutcher S., Irving N., MacSweeney C., Milne R., Mort C., Presland J., Sloan H., Thomson F., Turnbull Z., Young T.

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.

DOI

10.1016/j.bmcl.2011.02.096

Type

Journal article

Publication Date

2011-05-15T00:00:00+00:00

Volume

21

Pages

3163 - 3167

Total pages

4

Keywords

Amides, Antidiuretic Hormone Receptor Antagonists, Aza Compounds, Cells, Cultured, Cyclization, Drug Discovery, Humans, Liver, Molecular Structure, Protein Binding

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