The present invention provides novel C-linked cyclic compounds and analogues of Formula (I): ##STR00001## or a stereoisomer, tautomer, pharmaceutically acceptable salt or solvate form thereof, wherein the variables A, B, D and W are as defined herein. These compounds are selective inhibitors of the human P2Y.sub.1 receptor which can be used as medicaments.

 
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< 2-methoxymethyl-3-(3,4-dichlorophenyl)-8-azabicyclo[3.2.1]octane tartrate salts

> Heterocyclic compounds, methods for the preparation thereof, and uses thereof

> Phosphodiesterase 4 inhibitors

~ 00599