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 α7 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 α7 agonists as excellent leads for further evaluation is discussed, along with key physicochemical and pharmacokinetic data highlighting their lead potential. © 2009 Elsevier Ltd. All rights reserved.
Author supplied keywords
Cite
CITATION STYLE
O’Donnell, C. J., Peng, L., O’Neill, B. T., Arnold, E. P., Mather, R. J., Sands, S. B., … Nedza, F. M. (2009). Synthesis and SAR studies of 1,4-diazabicyclo[3.2.2]nonane phenyl carbamates - subtype selective, high affinity α7 nicotinic acetylcholine receptor agonists. Bioorganic and Medicinal Chemistry Letters, 19(16), 4747–4751. https://doi.org/10.1016/j.bmcl.2009.06.059
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.