Antitumor agents, 107. New cytotoxic 4-alkylamino analogues of 4'-demethyl-epipodophyllotoxin as inhibitors of human DNA topoisomerase II

J Nat Prod. 1989 May-Jun;52(3):606-13. doi: 10.1021/np50063a021.

Abstract

A series of analogues of etoposide, the C-4 amino- and alkylamino-substituted 4'-demethyl-epipodophyllotoxins, have been synthesized and studied for their activity to inhibit type II human DNA topoisomerase as well as their activity in causing cellular protein-linked DNA breakage. Substitution of the glycosidic moiety of 1 by a 2"-hydroxyethylamino or 2"-methoxyethylamino chain at the C-4 beta position resulted in potent inhibitors of the human DNA topoisomerase II. This inhibitory activity correlates reasonably well with their activity in causing protein-linked DNA breakage in KB cells. The in vitro cytotoxicity (KB) appears to have no correlation with the inhibitory activity of the human DNA topoisomerase II.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Cells, Cultured
  • DNA / drug effects
  • DNA Damage
  • Drug Screening Assays, Antitumor
  • Humans
  • Podophyllotoxin / analogs & derivatives*
  • Spectrum Analysis
  • Structure-Activity Relationship
  • Topoisomerase II Inhibitors*

Substances

  • Antineoplastic Agents
  • Topoisomerase II Inhibitors
  • DNA
  • Podophyllotoxin