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Novel glucocorticoids containing a 6,5-bicyclic core fused to a pyrazole ring: Synthesis, in vitro profile, molecular modeling studies, and in vivo experiments

  • Christopher F. Thompson
  • , Nazia Quraishi
  • , Amjad Ali
  • , Ralph T. Mosley
  • , James R. Tata
  • , Milton L. Hammond
  • , James M. Balkovec
  • , Monica Einstein
  • , Lan Ge
  • , Georgianna Harris
  • , Terri M. Kelly
  • , Paul Mazur
  • , Shilpa Pandit
  • , Joseph Santoro
  • , Ayesha Sitlani
  • , Chuanlin Wang
  • , Joanne Williamson
  • , Douglas K. Miller
  • , Ting ting D. Yamin
  • , Chris M. Thompson
  • Edward A. O'Neill, Dennis Zaller, Michael J. Forrest, Ester Carballo-Jane, Silvi Luell
  • Merck

Research output: Contribution to journal › Article › peer-review

18 Scopus citations

Abstract

Chemistry was developed to synthesize the title series of compounds. The ability of these novel ligands to bind to the glucocorticoid receptor was investigated. These compounds were also tested in a series of functional assays and some were found to display the profile of a dissociated glucocorticoid. The SAR of the 6,5-bicyclic series differed markedly from the previously reported 6,6-series. Molecular modeling studies were employed to understand the conformational differences between the two series of compounds, which may explain their divergent activity. Two compounds were profiled in vivo and shown to reduce inflammation in a mouse model. An active metabolite is suspected in one case.

Original languageEnglish
Pages (from-to)3354-3361
Number of pages8
JournalBioorganic and Medicinal Chemistry Letters
Volume17
Issue number12
DOIs
StatePublished - 15 Jun 2007

Keywords

  • Dissociation
  • Glucocorticoid
  • Inflammation
  • Transactivation
  • Transrepression

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