Synthesis of dihydrofuran-fused perhydrophenanthrenes having a phenolic hydroxyl group as a novel anti-Alzheimer's disease agent

Bioorg Med Chem Lett. 2012 Jan 1;22(1):449-52. doi: 10.1016/j.bmcl.2011.10.127. Epub 2011 Nov 18.

Abstract

As a part of our research program on developing novel anti-Alzheimer's disease medicines, several dihydrofuran-fused perhydrophenanthrenes (DFs) possessing a phenolic hydroxyl group were found to exhibit potent dendritic and axonal regeneration activities. Introduction of a methoxy group into the perhydrophenanthrene skeleton was successfully achieved via a PhI(OAc)(2)-mediated phenolic oxidation of a benzocyclobutene nucleus and subsequent tandem intramolecular electrocyclic reactions based on o-quinodimethane chemistry. We could reveal that a new methoxy derivative having a phenolic hydroxyl group exerted the most significant effects on the dendritic and axonal extensions in the damaged neurons, among DFs examined in this study.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Catechols / chemistry
  • Chemistry, Pharmaceutical / methods
  • Drug Design
  • Humans
  • Models, Chemical
  • Molecular Structure
  • Neutrons
  • Oxygen / chemistry
  • Phenanthrenes / chemistry*
  • Phenol / chemistry*
  • Phenols / chemistry

Substances

  • Catechols
  • Phenanthrenes
  • Phenols
  • Phenol
  • catechol
  • Oxygen