Abstract
A series of 1,6-naphthyridine-based compounds was synthesized as potent phosphodiesterase 10A (PDE10A) inhibitors. Structure-based chemical modifications of the discovered chemotype served to further improve potency and selectivity over DHODH, laying the foundation for future optimization efforts.
Copyright © 2012 Elsevier Ltd. All rights reserved.
MeSH terms
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Antipsychotic Agents / chemistry*
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Antipsychotic Agents / pharmacology*
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Humans
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Models, Molecular
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Naphthyridines / chemistry*
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Naphthyridines / pharmacology*
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Nitriles / chemistry
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Nitriles / pharmacology
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Phosphodiesterase Inhibitors / chemistry*
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Phosphodiesterase Inhibitors / pharmacology*
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Phosphoric Diester Hydrolases / chemistry
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Phosphoric Diester Hydrolases / metabolism*
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Structure-Activity Relationship
Substances
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Antipsychotic Agents
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Naphthyridines
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Nitriles
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Phosphodiesterase Inhibitors
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PDE10A protein, human
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Phosphoric Diester Hydrolases