Abstract
We describe an efficient and convergent synthesis of a series of (1'S,2R,4'S)-3H-4'-azaspiro[benzo[4,5]imidazo[2,1-b]oxazole-2,2'-bicyclo[2.2.2]octanes] displaying potency for the α7 nicotinic acetylcholine receptor (nAChR) and good selectivity vs. the related 5-HT3A receptor.
Keywords:
5-HT(3A) receptor; Schizophrenia; Spirooxazolines; α7 nicotinic acetylcholine receptor.
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MeSH terms
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Bridged Bicyclo Compounds / chemical synthesis
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Bridged Bicyclo Compounds / chemistry
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Bridged Bicyclo Compounds / metabolism*
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Crystallography, X-Ray
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Drug Design*
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Humans
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Hydrogen Bonding
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Molecular Conformation
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Nicotinic Agonists / chemistry
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Nicotinic Agonists / metabolism
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Octanes / chemical synthesis
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Octanes / chemistry
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Octanes / metabolism*
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Protein Binding
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Receptors, Serotonin, 5-HT3 / chemistry
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Receptors, Serotonin, 5-HT3 / metabolism
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Stereoisomerism
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alpha7 Nicotinic Acetylcholine Receptor / chemistry
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alpha7 Nicotinic Acetylcholine Receptor / metabolism*
Substances
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Bridged Bicyclo Compounds
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Nicotinic Agonists
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Octanes
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Receptors, Serotonin, 5-HT3
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alpha7 Nicotinic Acetylcholine Receptor
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bicyclo(2.2.2)octane