Article ID Journal Published Year Pages File Type
1363736 Bioorganic & Medicinal Chemistry Letters 2009 4 Pages PDF
Abstract

High-throughput screening of an encoded combinatorial aryl piperazine library led to the identification of a novel series of potent piperazinyl-piperidine based CXCR3 antagonists. Analogs of the initial hit were synthesized via solid and solution phase methods to probe the influence of structure on the CXCR3 binding of these molecules. Various functional groups were found to contribute to the overall potency and essential molecular features were identified.

Graphical abstractThe synthesis and SAR of a novel series of CXCR3 antagonists are reported.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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