Tautomerism in 11-hydroxyaklavinone: a DFT study

ScientificWorldJournal. 2012:2012:526289. doi: 10.1100/2012/526289. Epub 2012 May 1.

Abstract

The antharquinone-based chromophore of 11-hydroxyaklavinone is present in the structure of an anticancer agent, daunomycin. On the other hand, aklavinone is the parent aglycone of certain anthracycline antibiotics that possess anti-cancer activity too. The structures of aklavinone and its 11-hydroxy derivative have many -OH groups, and two keto groups which may take place in certain tautomeric equilibria. Of these tautomeric forms, presently the one involving the anthraquinone based tautomers of 11-hydroxyaklavinone has been investigated quantum chemically in the framework of the density functional theory at the levels of RB3LYP/6-31G(d) and RB3LYP/6-31G(d,p).

MeSH terms

  • Antineoplastic Agents / chemistry*
  • Chemical Phenomena
  • Daunorubicin / analogs & derivatives*
  • Daunorubicin / chemistry
  • Isomerism
  • Molecular Structure
  • Naphthacenes / chemistry
  • Quantum Theory
  • Spectrophotometry, Infrared

Substances

  • Antineoplastic Agents
  • Naphthacenes
  • aklavinone
  • Daunorubicin