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April 10, 2026Journal of Medicinal Chemistry0 citations

Development of Structurally Simplified, Non-azadecalin Glucocorticoid Antagonists which Demonstrate In Vivo Activity

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LDLorna DuffySignature Research (United States)MMMark MillsUniversity of MichiganAPAndrew W. PhillipsSignature Research (United States)

Key Points

  • To discover and optimize selective glucocorticoid receptor antagonists that are structurally simplified and demonstrate in vivo activity.
  • Discovery and optimization of piperazine-based GR antagonists
  • Utilization of insights from relacorilant
  • Progressing compounds to in vivo proof of concept studies
  • Identification of several compounds with desired profiles
  • Three key compounds advanced to in vivo studies
  • Demonstrated in vivo activity in select compounds

Abstract

Glucocorticoid receptor antagonists (GR antagonists) are a class of compounds developed to inhibit the activation of the glucocorticoid receptor and they have been used to treat a range of conditions such as Cushing's syndrome, diabetes, glaucoma, and depression. We report herein the discovery and optimization of a series of selective piperazine-based GR antagonists and discuss how key learnings from the discovery of relacorilant (CORT125134) were utilized to identify a simplified scaffold. Several compounds were identified with the desired profile and 3 key compounds were progressed to in vivo proof of concept studies.

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Cite This Study

Duffy et al. (2026) studied this question.

synapsesocial.com/papers/69d8948f6c1944d70ce0586chttps://doi.org/10.1021/acs.jmedchem.5c03567
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