Synthesis of 3-alkyl naphthalenes as novel estrogen receptor ligands

Bioorg Med Chem Lett. 2008 Sep 15;18(18):5075-7. doi: 10.1016/j.bmcl.2008.07.121. Epub 2008 Aug 5.

Abstract

A series of estrogen receptor ligands based on a 3-alkyl naphthalene scaffold was synthesized using an intramolecular enolate-alkyne cycloaromatization as the key step. Several of these compounds bearing a C6-OH group were shown to be high affinity ligands. All compounds had similar ERalpha and ERbeta binding affinity ranging from micromolar to low nanomolar.

MeSH terms

  • Combinatorial Chemistry Techniques
  • Estrogen Receptor Modulators / metabolism
  • Estrogen Receptor alpha / metabolism
  • Estrogen Receptor beta / metabolism
  • Female
  • Humans
  • Ligands
  • Molecular Structure
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / chemistry
  • Naphthalenes / pharmacology*
  • Receptors, Estrogen / agonists*
  • Selective Estrogen Receptor Modulators / metabolism
  • Structure-Activity Relationship

Substances

  • Estrogen Receptor Modulators
  • Estrogen Receptor alpha
  • Estrogen Receptor beta
  • Ligands
  • Naphthalenes
  • Receptors, Estrogen
  • Selective Estrogen Receptor Modulators