Identification of second-generation P2X3 antagonists for treatment of pain.

Bioorganic & Medicinal Chemistry Letters(2018)

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摘要
A second-generation small molecule P2X3 receptor antagonist has been developed. The lead optimization strategy to address shortcomings of the first-generation preclinical lead compound is described herein. These studies were directed towards the identification and amelioration of preclinical hepatobiliary findings, reducing potential for drug-drug interactions, and decreasing the projected human dose of the first-generation lead.
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关键词
P2X3,Pain,UGT1A1,Drug-drug interaction,Purinergic receptor
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