Article ID Journal Published Year Pages File Type
10594163 Bioorganic & Medicinal Chemistry Letters 2011 6 Pages PDF
Abstract
A series of 4-azetidinyl-1-aryl-cyclohexanes as potent CCR2 antagonists with high selectivity over activity for the hERG potassium channel is discovered through divergent SARs of CCR2 and hERG.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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