Diphenidol-related diamines as novel muscarinic M4 receptor antagonists

Bioorg Med Chem Lett. 2008 May 1;18(9):2972-6. doi: 10.1016/j.bmcl.2008.03.061. Epub 2008 Mar 23.

Abstract

A series of hydrochloride derivatives 2a-9a and quaternary ammonium derivatives 3b-9b of diphenidol have been synthesized and characterized in receptor binding and cellular functional assays versus human muscarinic M(1)-M(5) receptors expressed in CHO cells. Compound 8b, a methiodide derivative with a bipiperidinyl moiety and a second diphenidol framework, showed a potent and selective M(4) activity as competitive antagonist. Moreover 8b, acting as an allosteric modulator, was able to retard the dissociation rate of [(3)H]-N-methylscopolamine from CHO-M(4) cell membranes exposed to atropine. Taken together, these data suggest that 8b might open new avenues to the discovery of novel multivalent antagonists for the muscarinic receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allosteric Regulation
  • Animals
  • Binding, Competitive
  • CHO Cells
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Cricetinae
  • Cricetulus
  • Diamines / chemical synthesis
  • Diamines / pharmacology*
  • Humans
  • Kinetics
  • Muscarinic Antagonists / chemical synthesis
  • Muscarinic Antagonists / pharmacology*
  • N-Methylscopolamine / chemistry
  • Piperidines / chemistry
  • Piperidines / pharmacology*
  • Radioligand Assay
  • Receptor, Muscarinic M4 / antagonists & inhibitors*
  • Staining and Labeling
  • Structure-Activity Relationship

Substances

  • Diamines
  • Muscarinic Antagonists
  • Piperidines
  • Receptor, Muscarinic M4
  • diphenidol
  • N-Methylscopolamine