The design and synthesis of a novel series of indole derived selective ET(A) antagonists

Bioorg Med Chem Lett. 2002 Jan 21;12(2):125-8. doi: 10.1016/s0960-894x(01)00660-6.

Abstract

Conformational constraint has been used as the key design element in the identification of a series of potent and selective ET(A) antagonists. The most potent antagonist, 32, (ET(A) IC(50)=0.55nM) is 722-fold selective over the ET(B) receptor, as measured by binding experiments.

MeSH terms

  • Endothelin Receptor Antagonists*
  • Indoles / chemistry*
  • Indoles / pharmacology
  • Receptor, Endothelin A
  • Structure-Activity Relationship

Substances

  • Endothelin Receptor Antagonists
  • Indoles
  • Receptor, Endothelin A