Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10593279 | Bioorganic & Medicinal Chemistry Letters | 2013 | 5 Pages |
Abstract
A class of arylsulfonamide glucocorticoid receptor agonists that contains a substituted phenyl group as a steroid A-ring mimetic is reported. The structural design and SAR that provide the functional switching of a GR antagonist to an agonist is described. A combination of specific hydrogen bonding and lipophilic elements on the A-ring moiety is required to achieve potent GR agonist activity. This study culminated in the identification of compound 23 as a potent GR agonist with selectivity over the PR and MR nuclear hormone receptors.
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Organic Chemistry
Authors
Darren DiSalvo, Daniel Kuzmich, Jörg Bentzien, John Regan, Alison Kukulka, Tazmeen Fadra-Khan, Richard Nelson, Christian Harcken, David Thomson, Gerald Nabozny,