From bosentan (Tracleer®) to macitentan (Opsumit®): The medicinal chemistry perspective

Bioorg Med Chem Lett. 2016 Aug 1;26(15):3381-94. doi: 10.1016/j.bmcl.2016.06.014. Epub 2016 Jun 10.

Abstract

The endothelin peptides bind to two receptors found on cells of vasculature and in tissues. While the endothelin-A (ETA)-receptor is predominantly expressed in vascular smooth muscle cells, the endothelin-B (ETB)-receptor is also found in endothelial cells, fibroblasts, and neuronal cells. Activation of the endothelin system plays a driving role in several chronic cardiovascular diseases and several endothelin receptor antagonists (ERAs) (bosentan (6), ambrisentan (83) and macitentan (43)) have successfully been introduced as oral treatments for the life threatening condition of pulmonary arterial hypertension (PAH). This digest highlights the medicinal chemistry of the pyrimidine based ERAs 6 and 43 and describes the story that started with bosentan and culminated in macitentan (43). A condensed overview of the competitive landscape in the field of ERAs puts the different strategies and tactics applied by the medicinal chemists involved in this endeavor into perspective.

Keywords: Endothelin; Endothelin receptor antagonists (ERA); G-protein-coupled receptor (GPCR); Macitentan; Pulmonary arterial hypertension (PAH); Pyrimidine; Sulfamide.

Publication types

  • Review

MeSH terms

  • Bosentan
  • Chemistry, Pharmaceutical
  • Dose-Response Relationship, Drug
  • Humans
  • Molecular Structure
  • Pyrimidines / chemistry
  • Pyrimidines / pharmacology*
  • Receptors, Endothelin / metabolism*
  • Structure-Activity Relationship
  • Sulfonamides / chemistry
  • Sulfonamides / pharmacology*

Substances

  • Pyrimidines
  • Receptors, Endothelin
  • Sulfonamides
  • Bosentan
  • macitentan