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Discovery of Small Molecule Human FPR1 Receptor Antagonists

Bioorganic & medicinal chemistry letters(2011)

引用 27|浏览20
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摘要
The identification of two novel series of formyl peptide receptor 1 (FPR1) antagonists are reported, represented by methionine benzimidazole 6 and diamide 7. Both series specifically inhibited the binding of labelled fMLF to hrFPR1 and selectively antagonized FPR1 function in human neutrophils, making them useful in vitro validation tools for the target.
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关键词
FPR1 antagonist,Hit-to-lead,Small molecule
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