A Facile Oxidative Opening of the C-Ring in Luotonin A and Derivatives

Molecules. 2017 Sep 12;22(9):1540. doi: 10.3390/molecules22091540.

Abstract

An oxidative ring opening reaction of the central ring C in the alkaloid Luotonin A and two of its derivatives was found to occur upon heating with an excess amine and potassium carbonate in dimethylsulfoxide (DMSO) solution in the presence of air oxygen. The structure of the novel amide-type products was elucidated and a possible mechanism for this reaction is proposed. Four of the new compounds show moderate in vitro anticancer activity towards human colon adenocarcinoma cells.

Keywords: Luotonin A; anticancer activity; oxidation; quinazoline; quinoline; ring opening.

MeSH terms

  • Antineoplastic Agents / chemical synthesis
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Cell Line, Tumor
  • Humans
  • Magnetic Resonance Spectroscopy
  • Mass Spectrometry
  • Molecular Structure
  • Oxidation-Reduction*
  • Pyrroles / chemical synthesis
  • Pyrroles / chemistry*
  • Pyrroles / pharmacology
  • Quinones / chemical synthesis
  • Quinones / chemistry*
  • Quinones / pharmacology

Substances

  • Antineoplastic Agents
  • Pyrroles
  • Quinones
  • luotonin A