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Synthesis and Pharmacological Characterization ofTwo Novel Brain Penetrating P2X7 Antagonists

机译:of的合成与药理表征两种新颖的能穿透大脑的P2X7拮抗剂

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摘要

The synthesis and preclinical characterization of two novel, brain penetrating P2X7 compounds will be described. Both compounds are shown to be high potency P2X7 antagonists in human, rat, and mouse cell lines and both were shown to have high brain concentrations and robust receptor occupancy in rat. Compound >7 is of particular interest as a probe compound for the preclinical assessment of P2X7 blockade in animal models of neuro-inflammation.
机译:将描述两种新颖的可穿透脑的P2X7化合物的合成和临床前表征。两种化合物在人,大鼠和小鼠细胞系中均显示为高效P2X7拮抗剂,在大鼠中均显示出较高的脑浓度和强大的受体占有率。化合物> 7 作为神经炎症动物模型中P2X7阻断的临床前评估的探针化合物特别受关注。

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