Synthesis and Biological Activity of AllostericModulators of GABAB Receptors, Part 1. N-(Phenylpropyl)-1-arylethylamines*
David I. B. Kerr A C , Jennifer Ong A , Michael V. Perkins B , Rolf H. Prager B D and Ni Made Puspawati BA Department of Anaesthesia and Intensive Care, University of Adelaide, Adelaide SA 5005, Australia.
B School of Chemistry, Physics and Earth Sciences, Flinders University, Adelaide SA 5001, Australia.
C Deceased, July 2005.
D Corresponding author. Email: rolf.prager@flinders.edu.au
Australian Journal of Chemistry 59(7) 445-456 https://doi.org/10.1071/CH06163
Submitted: 15 May 2006 Accepted: 5 July 2006 Published: 22 August 2006
Abstract
A series of 15 analogues of fendiline, and 34 derivatives of N-(3-phenylpropyl)-1-arylethylamine have been prepared for evaluation as positive allosteric modulators of GABAB receptors. The most active (EC50, 10 nM) was N-(3,3-diphenylpropyl)-1-(3-chloro-4-methoxyphenyl)ethylamine 6g.
Acknowledgments
N.M.P. is grateful for the award of an overseas scholarship from Austaid.
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* Part 2: D. I. B. Kerr, J. Khalafy, J. Ong, M. V. Perkins, R. H. Prager, N. M. Puspawati, M. Rimaz, Aust. J. Chem. 2006, 59, 457. doi:10.1071/CH06164