Esters and amides of 2,3-dimethoxy-8,9-methylenedioxy-benzo[i]phenanthridine-12-carboxylic acid: potent cytotoxic and topoisomerase I-targeting agents

Bioorg Med Chem. 2005 Dec 15;13(24):6782-94. doi: 10.1016/j.bmc.2005.07.033. Epub 2005 Sep 8.

Abstract

The exceptional topoisomerase I-targeting activity and antitumor activity of 5-(2-N,N-dimethylamino)ethyl-8,9-dimethoxy-2,3-methylenedioxy-5H-dibenzo[c,h][1,6]naphthyridin-6-one (ARC-111, topovale) prompted studies on similarly substituted benzo[i]phenanthridine-12-carboxylic ester and amide derivatives. Among the benzo[i]phenanthridine-12-carboxylic esters evaluated, the 2-(N,N-dimethylamino)ethyl, 2-(N,N-dimethylamino)-1-methylethyl, and 2-(N,N-dimethylamino)-1,1-dimethylethyl esters possessed similar cytotoxicity, ranging from 30 to 55 nM in RPMI8402 and KB3-1 cells. Several of the carboxamide derivatives possess potent topoisomerase I-targeting activity and cytotoxicity. The 2-(N,N-dimethylamino)ethyl, 2-(N,N-diethylamino)ethyl, and 2-(pyrrolidin-1-yl)ethyl amides were among the more cytotoxic benzo[i]phenanthridine-12-carboxylic derivatives, with IC50 values ranging from 0.4 to 5.0 nM in RPMI8402 and KB3-1 cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amides / chemistry*
  • Camptothecin / analogs & derivatives
  • Camptothecin / chemistry
  • Cell Line
  • Cell Survival / drug effects
  • DNA / metabolism
  • DNA Topoisomerases, Type I / metabolism
  • Enzyme Inhibitors / chemical synthesis
  • Enzyme Inhibitors / chemistry*
  • Enzyme Inhibitors / toxicity*
  • Esters / chemistry*
  • Humans
  • Inhibitory Concentration 50
  • Irinotecan
  • Molecular Structure
  • Topoisomerase I Inhibitors*
  • Topotecan / chemistry

Substances

  • Amides
  • Enzyme Inhibitors
  • Esters
  • Topoisomerase I Inhibitors
  • Irinotecan
  • Topotecan
  • DNA
  • DNA Topoisomerases, Type I
  • Camptothecin