Bioorganic and Medicinal Chemistry Letters p. 3025 - 3028 (1996)
Update date:2022-08-11
Topics:
Bisel, Philippe
Gies, Jean Pierre
Schlewer, Gilbert
Wermuth, Camille G.
6-(4-Phenyl-benzyloxy-methyl) guvacine was synthesized. Surprisingly the compound was devoid of the γ-aminobutyric acid (GABA) uptake inhibitory activity of its parent compound guvacine, but instead showed affinities for the muscarinic M1 and M2 receptors.
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