Article ID Journal Published Year Pages File Type
10588622 Bioorganic & Medicinal Chemistry Letters 2011 4 Pages PDF
Abstract
High-throughput screening of 3.87 million compounds delivered a novel series of non-steroidal GR antagonists. Subsequent rounds of optimisation allowed progression from a non-selective ligand with a poor ADMET profile to an orally bioavailable, selective, stable, glucocorticoid receptor antagonist.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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