Ferrocenyl quinone methides as strong antiproliferative agents: formation by metabolic and chemical oxidation of ferrocenyl phenols

Angew Chem Int Ed Engl. 2009;48(48):9124-6. doi: 10.1002/anie.200903768.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Ferrous Compounds / chemistry*
  • Humans
  • Indolequinones / chemical synthesis*
  • Indolequinones / metabolism
  • Indolequinones / pharmacology*
  • Metallocenes
  • Models, Molecular
  • Molecular Structure
  • Oxidation-Reduction
  • Phenols / chemistry*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Ferrous Compounds
  • Indolequinones
  • Metallocenes
  • Phenols
  • quinone methide
  • ferrocene