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Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/22732
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dc.contributor.authorKerr, D.-
dc.contributor.authorOng, J.-
dc.contributor.authorPerkins, M.-
dc.contributor.authorPrager, R.-
dc.contributor.authorPuspawati, N.-
dc.date.issued2006-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 2006; 59(7):445-456-
dc.identifier.issn0004-9425-
dc.identifier.urihttp://hdl.handle.net/2440/22732-
dc.description.abstract<jats:p> 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. </jats:p>-
dc.language.isoen-
dc.publisherC S I R O Publishing-
dc.source.urihttp://dx.doi.org/10.1071/ch06163-
dc.titleSynthesis and biological activity of allosteric modulators of GABA(B) receptors, Part 1. N-(phenylpropyl)-1-arylethylamines-
dc.typeJournal article-
dc.identifier.doi10.1071/CH06163-
pubs.publication-statusPublished-
dc.identifier.orcidOng, J. [0000-0002-0958-460X]-
Appears in Collections:Anaesthesia and Intensive Care publications
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