Abstract
Structure-activity relationships (SAR) of a weakly active class of CCR2b inhibitors were utilized to initiate a lead evolution program employing the Drug Discovery Engine. Several alternative structural series have been discovered that display nanomolar activity in the CCR2b binding and CCR2b-mediated chemotaxis assays.
MeSH terms
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Cell Line
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Chemokine CCL2 / metabolism
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Chemotaxis / drug effects
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Combinatorial Chemistry Techniques
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Diamines / chemical synthesis*
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Diamines / chemistry
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Diamines / pharmacology
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Drug Design
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Humans
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Piperidines / chemical synthesis
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Piperidines / chemistry
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Piperidines / pharmacology
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Pyrrolidines / chemical synthesis
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Pyrrolidines / chemistry
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Pyrrolidines / pharmacology
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Radioligand Assay
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Receptors, CCR2
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Receptors, Chemokine / antagonists & inhibitors*
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Structure-Activity Relationship
Substances
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CCR2 protein, human
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Chemokine CCL2
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Diamines
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Piperidines
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Pyrrolidines
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Receptors, CCR2
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Receptors, Chemokine