Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/22733
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dc.contributor.authorKerr, D.-
dc.contributor.authorKhalafy, J.-
dc.contributor.authorOng, J.-
dc.contributor.authorPerkins, M.-
dc.contributor.authorPrager, R.-
dc.contributor.authorPuspawati, N.-
dc.contributor.authorRimaz, M.-
dc.date.issued2006-
dc.identifier.citationAustralian Journal of Chemistry: an international journal for chemical science, 2006; 59(7):457-462-
dc.identifier.issn0004-9425-
dc.identifier.urihttp://hdl.handle.net/2440/22733-
dc.description.abstractA series of 13 2,2-disubstituted 3-(3,5-di-t-butyl-4-hydroxyphenyl)propan-1-ol derivatives have been prepared for evaluation as allosteric modulators of GABAB receptors. The activity (EC50, 4–7 μM) was greatest for the cyclohexyl and cyclopentyl analogues.-
dc.description.statementofresponsibilityDavid I. B. Kerr, Jabbar Khalafy, Jennifer Ong, Michael V. Perkins, Rolf H. Prager, Ni Made Puspawati and Mehdi Rimaz-
dc.language.isoen-
dc.publisherC S I R O Publishing-
dc.rights© CSIRO 2006-
dc.source.urihttp://dx.doi.org/10.1071/ch06164-
dc.titleSynthesis and biological activity of allosteric modulators of GABA(B) receptors, Part 2. 3-(2,6-bis-tert-butyl-4-hydroxyphenyl)propanols-
dc.typeJournal article-
dc.identifier.doi10.1071/CH06164-
pubs.publication-statusPublished-
dc.identifier.orcidOng, J. [0000-0002-0958-460X]-
Appears in Collections:Anaesthesia and Intensive Care publications
Aurora harvest 6

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