Literature DB >> 19576766

Synthesis and SAR studies of 1,4-diazabicyclo[3.2.2]nonane phenyl carbamates--subtype selective, high affinity alpha7 nicotinic acetylcholine receptor agonists.

Christopher J O'Donnell1, Langu Peng, Brian T O'Neill, Eric P Arnold, Robert J Mather, Steven B Sands, Alka Shrikhande, Lorraine A Lebel, Douglas K Spracklin, Frank M Nedza.   

Abstract

The synthesis and SAR studies about the bicyclic amine, carbamate linker and aromatic ring of a 1,4-diazabicyclo[3.2.2]nonane phenyl carbamate series of alpha7 nAChR agonists is described. The development of the medicinal chemistry strategy and SAR which led to the identification of 5 and 7aa as subtype selective, high affinity alpha7 agonists as excellent leads for further evaluation is discussed, along with key physicochemical and pharmacokinetic data highlighting their lead potential.

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Year:  2009        PMID: 19576766     DOI: 10.1016/j.bmcl.2009.06.059

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

Review 1.  Cancer 'survivor-care': I. the α7 nAChR as potential target for chemotherapy-related cognitive impairment.

Authors:  R B Raffa
Journal:  J Clin Pharm Ther       Date:  2010-08-24       Impact factor: 2.512

2.  The 3,7-diazabicyclo[3.3.1]nonane scaffold for subtype selective nicotinic acetylcholine receptor (nAChR) ligands. Part 1: the influence of different hydrogen bond acceptor systems on alkyl and (hetero)aryl substituents.

Authors:  Christoph Eibl; Isabelle Tomassoli; Lenka Munoz; Clare Stokes; Roger L Papke; Daniela Gündisch
Journal:  Bioorg Med Chem       Date:  2013-10-05       Impact factor: 3.641

  2 in total

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