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Bioorg Med Chem Lett ; 20(16): 4749-52, 2010 Aug 15.
Article in English | MEDLINE | ID: mdl-20663668

ABSTRACT

We report the synthesis of a series of [3.2.1]azabicyclic biaryl ethers as selective agonists of alpha3- and alpha6-containing nicotinic receptors. In particular, compound 17a from this series is a potent alpha3beta4 and alpha6/4beta4 receptor agonist in terms of both binding and functional activity. Compound 17a also shows potent in vivo activity in CNS-mediated animal models that are sensitive to antipsychotic drugs. Compound 17a may thus be a useful tool for studying the role of alpha3beta4 and alpha6/4beta4 nicotinic receptors in CNS pharmacology.


Subject(s)
Azabicyclo Compounds/chemistry , Nicotinic Agonists/chemistry , Receptors, Nicotinic/chemistry , Sulfonamides/chemistry , Azabicyclo Compounds/chemical synthesis , Azabicyclo Compounds/pharmacology , Nicotinic Agonists/chemical synthesis , Nicotinic Agonists/pharmacology , Receptors, Nicotinic/metabolism , Structure-Activity Relationship , Sulfonamides/chemical synthesis , Sulfonamides/pharmacology
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