Synthesis and biological evaluation of new spin-labeled derivatives of podophyllotoxin

Bioorg Med Chem. 2006 May 1;14(9):3062-8. doi: 10.1016/j.bmc.2005.12.025. Epub 2006 Jan 9.

Abstract

In order to find compounds with superior bioactivity and less toxicity, a series of spin-labeled podophyllotoxin derivatives were synthesized and tested for the partition coefficients and cytotoxicity against P-388 and A-549. Furthermore, we also determined antioxidant activities of target molecular in tissues of SD rats by the TBA method. Results revealed that most synthesized compounds showed more significant cytotoxicity against P-388 and A-549 in vitro than VP-16. Among them, 9d exhibited most potent cytotoxicity against P-388 and A-549 cells (IC50 is <0.01 and 0.13 microM, respectively). Also, the antioxidative activities showed that the modified compounds of 4'-demethylepipodophyllotoxin (9a-d and 10a-c) are higher than those of podophyllotoxin series (8a-d). The relationship between the cytotoxicity and antioxidative activity discussed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / chemical synthesis
  • Antioxidants / chemistry
  • Antioxidants / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Molecular Structure
  • Podophyllotoxin / chemical synthesis
  • Podophyllotoxin / chemistry*
  • Podophyllotoxin / pharmacology*
  • Structure-Activity Relationship

Substances

  • Antioxidants
  • Podophyllotoxin