Benzothiophene and naphthalene derived constrained SERMs

Bioorg Med Chem Lett. 2004 Oct 18;14(20):5103-6. doi: 10.1016/j.bmcl.2004.07.072.

Abstract

For selective estrogen receptor modulators (SERMs), the orientation of the basic side chain relative to the SERM core has a significant impact on function. The synthesis and biological evaluation of two series of SERMs are disclosed, where the ligand side chain is constrained to adopt a defined orientation. Compounds where the side chain is forced into the plane of the SERM core have a different profile compared to those compounds where the side chain is pseudo-orthogonal, particularly with regard to antagonism of estradiol action on an Ishikawa uterine cell line.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Cell Line
  • Chromatography, High Pressure Liquid
  • Female
  • Humans
  • Ligands
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / chemistry
  • Naphthalenes / pharmacology
  • Radioligand Assay
  • Rats
  • Selective Estrogen Receptor Modulators / chemical synthesis*
  • Selective Estrogen Receptor Modulators / chemistry
  • Selective Estrogen Receptor Modulators / pharmacology
  • Structure-Activity Relationship
  • Thiophenes / chemical synthesis*
  • Thiophenes / chemistry
  • Thiophenes / pharmacology
  • Uterus / drug effects
  • Uterus / physiology

Substances

  • Ligands
  • Naphthalenes
  • Selective Estrogen Receptor Modulators
  • Thiophenes
  • benzothiophene