Pyridyl amides as potent inhibitors of T-type calcium channels.

Bioorganic & Medicinal Chemistry Letters(2011)

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摘要
A novel series of amide T-type calcium channel antagonists were prepared and evaluated using in vitro and in vivo assays. Optimization of the screening hit 3 led to identification of the potent and selective T-type antagonist 37 that displayed in vivo efficacy in rodent models of epilepsy and sleep.
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关键词
T-type calcium channel,Structure–activity relationships,Pregnane X receptor,Electrocorticogram,Epilepsy
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