New series of N-substituted phenyl ketone oxime ethers: synthesis and bovine beta3-adrenergic agonistic activities.

A series of ten novel phenyl ketone oxime ethers substituted on the terminal nitrogen by either 1,3 benzodioxole, alkyl, aralkyl or aryl moiety were synthesized and tested for their activity at bovine β 3 -adrenoceptors. The best compound, which was the benzodioxole dicarboxylate derivative, showed potent β 3 -adrenergic agonistic activities in Chinese hamster ovary cells expressing the bovine,83-adrenoceptors with K act and K i values better than compound CL 316,243 used as reference (14 ± 6 nM and 203 ± 71 nM, respectively). In this series three compounds showed an antagonistic activity. Structure-activity relationships in these ketone oxime ethers are discussed.