Discovery of the first low-shift positive allosteric modulators for the muscarinic M1 receptor

Bioorg Med Chem Lett. 2017 Dec 15;27(24):5415-5419. doi: 10.1016/j.bmcl.2017.11.008. Epub 2017 Nov 6.

Abstract

Positive modulation of the muscarinic M1-receptor has for a long time attracted scientists and drug developers for the potential treatment of Alzheimer's disease or Schizophrenia. The precognitive potential of M1 activation has however not been clinically demonstrated as a result of side effects associated both with agonists and positive allosteric modulators (PAM's) of the M1-receptor. To avoid excessive activation of the M1-receptor we have designed a new screening format and developed the first low-shift positive allosteric modulators for the M1 receptor. Low-shift PAM's offer the potential of "use-dependent" attenuation of transmitter-signaling while avoiding pseudo-agonistic behavior in vivo as a common limitation of the so far described high-shift PAM's. With these novel M1-PAM's, the M1 receptor is potentially the first GPCR for which both, high- and low shift PAM's have become available.

Keywords: Allosteric; Cognition; GPCR; M1; Modulator; Muscarinic.

MeSH terms

  • Allosteric Regulation
  • Animals
  • CHO Cells
  • Cricetinae
  • Cricetulus
  • Drug Evaluation, Preclinical
  • GABA-A Receptor Agonists / chemistry
  • GABA-A Receptor Agonists / metabolism
  • Humans
  • Muscarinic Agonists / chemistry
  • Mutagenesis, Site-Directed
  • Receptor, Muscarinic M1 / chemistry
  • Receptor, Muscarinic M1 / genetics
  • Receptor, Muscarinic M1 / metabolism*
  • Receptors, GABA-A / chemistry
  • Receptors, GABA-A / metabolism
  • Structure-Activity Relationship

Substances

  • GABA-A Receptor Agonists
  • Muscarinic Agonists
  • Receptor, Muscarinic M1
  • Receptors, GABA-A