Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1363736 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
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
Authors
Brian F. McGuinness, Carolyn DiIanni Carroll, Lisa Guise Zawacki, Guizhen Dong, Cangming Yang, Doug W. Hobbs, Biji Jacob-Samuel, James W. Hall III, Chung-Her Jenh, Joseph A. Kozlowski, Gopinadhan N. Anilkumar, Stuart B. Rosenblum,