Identification of a new scaffold for opioid receptor antagonism based on the 2-amino-1,1-dimethyl-7-hydroxytetralin pharmacophore

Peter Grundt, Ian A. Williams, John W. Lewis, Stephen M. Husbands

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The trans-(3,4)-dimethyl-4-(3-hydroxyphenyl)piperidines are a unique class of opioid antagonists that have recently provided selective antagonists for μ-opioid receptors (MOR) and κ-opioid receptors (KOR). Molecular modeling indicated a strong structural similarity between the parent of this series and 2-amino-1,1-dimethyl-7-hydroxytetralin. In binding and in vitro functional assays, the aminotetralin derivatives displayed some overlap in SAR with that previously reported for the phenylpiperidine series, providing evidence for a common binding mode for the two series at opioid receptors. Introduction of a methoxy group in the 3-position increased potency at MOR and KOR receptors, suggesting that this aminotetralin skeleton can be utilized as a new scaffold for the design of selective opioid receptor antagonists.

Original languageEnglish (US)
Pages (from-to)5069-5075
Number of pages7
JournalJournal of Medicinal Chemistry
Volume47
Issue number21
DOIs
StatePublished - Oct 7 2004

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