Contribution of monofunctional adducts formed by furocoumarins with DNA to the inhibition of nucleic acids synthesis

Z Naturforsch C Biosci. 1976 Mar-Apr;31(3-4):207-8. doi: 10.1515/znc-1976-3-425.

Abstract

In addition to the bifunctional adducts (cross-linkages), that furocoumarins on radiation at 365 nm form in DNA, monofunctional adducts also proved able to inhibit the nucleic acid synthesis in Ehrlich ascites tumor cells.

MeSH terms

  • Cell Line
  • Coumarins / pharmacology*
  • DNA / biosynthesis*
  • Ficusin / pharmacology
  • Furocoumarins
  • Photochemistry
  • RNA / biosynthesis*
  • Structure-Activity Relationship
  • Ultraviolet Rays

Substances

  • Coumarins
  • Furocoumarins
  • RNA
  • DNA
  • Ficusin