4.7 Article

Guanidine and 2-aminoimidazoline aromatic derivatives as α2-adrenoceptor antagonists.: 2.: Exploring alkyl linkers for new antidepressants

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 51, Issue 11, Pages 3304-3312

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm800026x

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The preparation of a number of (bis)ouanidine and (bis)2-aminoimidazoline derivatives as potential alpha(2)-adrenoceptor antagonists for the treatment of depression is presented. Human brain tissue was used to measure their affinity toward the alpha(2)-adrenoceptors in vitro. Compounds 6b, 8b, 9b, 10b, 15b, 17b, 18b, 20b, and 21b displayed a good affinity (pK(i) > 7) and were evaluated in in vitro functional [(35)S]GTP gamma S binding assays in human prefrontal cortex to determine their agonistic or antagonistic activity. Among these compounds, 17b and 20b showed the expected behavior for an antagonist and were subject to in vivo microdialysis experiments in rats. Significantly, these experiments confirmed the antagonistic properties of 17b and 20b, and therefore both compounds can be considered as potential antidepressants.

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