Abstract
The preparation and biological activity of analogs of (-)-cytisine, an alpha4beta2 nicotinic receptor partial agonist, are discussed. All-carbon-containing phenyl ring replacements of the pyridone ring system, generated via Heck cyclization protocols, exhibited weaker affinity and lower efficacy partial agonist profiles relative to (-)-cytisine. In vivo, selected compounds exhibit lower efficacy partial agonist profiles than that of (-)-cytisine.
MeSH terms
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Alkaloids / chemistry
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Alkaloids / pharmacology*
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Animals
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Azocines / chemistry
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Azocines / pharmacology
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Carbon / chemistry*
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Dopamine / metabolism*
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Nicotinic Agonists / chemistry
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Nicotinic Agonists / pharmacology*
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Nucleus Accumbens / drug effects*
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Quinolizines / chemistry
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Quinolizines / pharmacology
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Rats
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Receptors, Nicotinic / chemistry*
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Receptors, Nicotinic / metabolism
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Smoking Cessation
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Structure-Activity Relationship
Substances
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Alkaloids
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Azocines
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Nicotinic Agonists
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Quinolizines
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Receptors, Nicotinic
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nicotinic receptor alpha4beta2
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cytisine
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Carbon
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Dopamine