Structure–activity relationship studies of novel 3-oxazolidinedione-6-naphthyl-2-pyridinones as potent and orally bioavailable EP3 receptor antagonists

Bioorganic & Medicinal Chemistry Letters(2011)

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摘要
3-Oxazolidinedione-6-napthyl-2-pyridinones are presented as novel and subtype selective EP3 antagonists. The synthesis and extensive SAR that led to the discovery of compound 29 are described.
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关键词
EP3 receptor,Novel, potent, selective, and orally active antagonists,3-Oxazolidinedione-6-aryl-pyridinones
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