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Bioorg Med Chem Lett ; 15(13): 3229-32, 2005 Jul 01.
Article in English | MEDLINE | ID: mdl-15936190

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.


Subject(s)
Pyrrolidines/chemical synthesis , Receptors, G-Protein-Coupled/antagonists & inhibitors , Drug Evaluation, Preclinical , Humans , Pyrrolidines/pharmacology , Stereoisomerism , Structure-Activity Relationship
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