Antitrypanosomal activity of quaternary naphthalimide derivatives

Bioorg Med Chem Lett. 2007 Mar 15;17(6):1590-3. doi: 10.1016/j.bmcl.2006.12.088. Epub 2007 Jan 4.

Abstract

Sleeping sickness caused by Trypanosoma brucei gambiense and rhodesiense is fatal if left untreated. Due to the toxicity of drugs currently used and the emerging resistance against these drugs new lead compounds are urgently needed. Within the frame of a broad screening program for drugs with antitrypanosomal activity, some highly potent tertiary and quaternary mono- and bisnaphthalimides being active in the lower micromolar and nanomolar range of concentration have been identified. These compounds are easily available via a two- or three-step microwave-driven synthesis with high yield.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drug Evaluation, Preclinical
  • Humans
  • Indicators and Reagents
  • Mice
  • Naphthalimides / chemical synthesis*
  • Naphthalimides / pharmacology*
  • Structure-Activity Relationship
  • Trypanocidal Agents / chemical synthesis*
  • Trypanocidal Agents / pharmacology*
  • Trypanosoma brucei brucei / drug effects

Substances

  • Indicators and Reagents
  • Naphthalimides
  • Trypanocidal Agents