Abstract
SAR studies were conducted around lead compound 1 using high-throughput parallel solution and solid phase synthesis. Our lead optimization efforts led to the identification of several CCR2b antagonists with potent activity in both binding and functional assays [Compound 71 CCR2b Binding IC(50) 3.2 nM; MCP-1-Induced Chemotaxis IC(50) 0.83 nM; Ca(2+) Flux IC(50) 7.5 nM].
MeSH terms
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Calcium / metabolism
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Cells, Cultured
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Chemokine CCL2 / metabolism*
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Chemotaxis / drug effects*
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Chromatography, High Pressure Liquid
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Fluorescence
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Humans
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Kidney / cytology
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Kidney / drug effects
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Kidney / metabolism
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Molecular Structure
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Monocytes / drug effects
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Monocytes / metabolism
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Pyrrolidines / chemical synthesis
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Pyrrolidines / pharmacology*
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Receptors, CCR2 / antagonists & inhibitors*
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Receptors, CCR2 / metabolism
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Structure-Activity Relationship
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Transfection
Substances
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CCL2 protein, human
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CCR2 protein, human
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Chemokine CCL2
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Pyrrolidines
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Receptors, CCR2
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Calcium