Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1375720 | Bioorganic & Medicinal Chemistry Letters | 2005 | 4 Pages |
Abstract
High throughput screening of the corporate compound collection led to the discovery of a novel series of substituted aminoalkoxybenzyl pyrrolidines as human urotensin-II receptor antagonists. The synthesis, initial structure-activity relationships, and optimization of the initial hit that led to the identification of a truncated sub-series, represented by SB-436811 (1a), are described.
Related Topics
Physical Sciences and Engineering
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Authors
Jian Jin, Dashyant Dhanak, Steven D. Knight, Katherine Widdowson, Nambi Aiyar, Diane Naselsky, Henry M. Sarau, James J. Foley, Dulcie B. Schmidt, Carl D. Bennett, Bing Wang, Gregory L. Warren, Michael L. Moore, Richard M. Keenan, Ralph A. Rivero,