Article ID Journal Published Year Pages File Type
1375720 Bioorganic & Medicinal Chemistry Letters 2005 4 Pages PDF
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 Chemistry Organic Chemistry
Authors
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