Novel substituted tetrahydrotriazaacenaphthylene derivatives as potent CRF1 receptor antagonists

Bioorg Med Chem Lett. 2007 Sep 15;17(18):5218-21. doi: 10.1016/j.bmcl.2007.06.077. Epub 2007 Jun 30.

Abstract

Corticotropin-releasing factor (CRF), a 41 amino acid peptide neurohormone synthesised by specific hypothalamic nuclei in the brain, is implicated in stress-related function. Antagonism of CRF(1) receptors is an attractive therapeutic approach for the treatment of depression and anxiety. Unsaturated tetrahydrotriazaacenaphthylenes of general structure 3 have been identified as potent and selective CRF(1) receptor antagonists with a suitable oral pharmacokinetic profile.

MeSH terms

  • Administration, Oral
  • Humans
  • Naphthalenes / administration & dosage
  • Naphthalenes / chemistry
  • Naphthalenes / pharmacokinetics
  • Naphthalenes / pharmacology*
  • Receptors, Corticotropin-Releasing Hormone / antagonists & inhibitors*
  • Recombinant Proteins / antagonists & inhibitors

Substances

  • Naphthalenes
  • Receptors, Corticotropin-Releasing Hormone
  • Recombinant Proteins
  • CRF receptor type 1