Potent antitumor activity of synthetic 1,2-Naphthoquinones and 1,4-Naphthoquinones

Bioorg Med Chem. 2003 Jul 17;11(14):3179-91. doi: 10.1016/s0968-0896(03)00226-8.

Abstract

Rhinacanthone (1) and two 1,2-pyranonaphthoquinones (2,3) were synthesized and found to show very potent cytotoxicity against three cancer cell lines (KB, HeLa and HepG(2)) with IC(50) values of 0.92-9.63 microM, whereas the corresponding hydroxylated derivative 4 had reduced cytotoxicity (IC(50) values of 7.61-24.13 microM). Three 1,2-furanonaphthoquinone derivatives (5-7) were also synthesized with similar cytotoxicity as 1,2-pyranonaphthoquinones. In comparison to 1,2-naphthoquinones, six 1,4-naphthoquinones derivatives fused with pyran ring (8-10) and furan ring (11-13) were synthesized and they showed less cytotoxicity or inactive to the cancer cell lines. Moreover, compound 13 had significant cytotoxicity against HeLa cell line (IC(50) value of 9.25 microM) while it showed no toxic to vero cell.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology
  • Benzopyrans / chemical synthesis
  • Benzopyrans / pharmacology
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Furans / chemistry
  • Humans
  • Molecular Structure
  • Naphthoquinones / chemical synthesis*
  • Naphthoquinones / pharmacology
  • Pyrans / chemistry

Substances

  • Antineoplastic Agents
  • Benzopyrans
  • Furans
  • Naphthoquinones
  • Pyrans
  • rhinacanthone