Indazole derivatives as novel bradykinin B1 receptor antagonists.
Bioorganic & Medicinal Chemistry Letters(2010)
摘要
A new class of indazole-derived bradykinin B1 antagonists and their structure–activity relationships (SAR) is reported. A number of compounds were found to have low-nanomolar affinity for the human B1 receptor and possess acceptable P-gp and pharmacokinetics properties.
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关键词
Bradykinin,Antagonist,Indazole,P-Glycoprotein
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