1. Academic Validation
  2. Structure-activity relationship, biological, and pharmacological characterization of the proline sulfonamide ACT-462206: a potent, brain-penetrant dual orexin 1/orexin 2 receptor antagonist

Structure-activity relationship, biological, and pharmacological characterization of the proline sulfonamide ACT-462206: a potent, brain-penetrant dual orexin 1/orexin 2 receptor antagonist

  • ChemMedChem. 2014 Nov;9(11):2486-96. doi: 10.1002/cmdc.201402258.
Christoph Boss 1 Catherine Roch-Brisbare Michel A Steiner Alexander Treiber Hendrik Dietrich Francois Jenck Markus von Raumer Thierry Sifferlen Christine Brotschi Bibia Heidmann Jodi T Williams Hamed Aissaoui Romain Siegrist John Gatfield
Affiliations

Affiliation

  • 1 Drug Discovery and Preclinical Research & Development, Actelion Pharmaceuticals Ltd. Gewerbestrasse 16, 4123 Allschwil/BL (Switzerland). [email protected].
Abstract

The orexin system consists of two G-protein-coupled receptors, the orexin 1 and orexin 2 receptors, widely expressed in diverse regions of the brain, and two peptide agonists, orexin A and orexin B, which are produced in a small assembly of neurons in the lateral hypothalamus. The orexin system plays an important role in the maintenance of wakefulness. Several compounds (almorexant, SB-649868, suvorexant) have been in advanced clinical trials for treating primary insomnia. ACT-462206 is a new, potent, and selective dual orexin receptor antagonist (DORA) that inhibits the stimulating effects of the orexin Peptides at both the orexin 1 and 2 receptors. It decreases wakefulness and increases non-rapid eye movement (non-REM) and REM sleep while maintaining natural sleep architectures in rat and dog electroencephalography/electromyography (EEG/EMG) experiments. ACT-462206 shows anxiolytic-like properties in rats without affecting cognition and motor function. It is therefore a potential candidate for the treatment of insomnia.

Keywords

insomnia; neurotransmitters; orexin receptor antagonists; peptides; stress-related disorders.

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