Photo-induced DNA cleavage reaction characteristics of propargylic sulfones possessing anthraquinone chromophore

Bioorg Med Chem. 2003 Dec 1;11(24):5311-6. doi: 10.1016/j.bmc.2003.09.030.

Abstract

DNA cleavage potency of propargylic sulfones possessing anthraquinone chromophore 1 under UV-irradiation was evaluated in comparison with the dark reaction. 1 showed inefficient DNA cleavage activity, while having considerably strong DNA binding ability. This result is accounted for by spatial conditions that the activated alkylating allenic site of intercalated 1 could not effectively approach to DNA bases, most probably guanine moiety, and thereby led to insufficient DNA strand cleavage. In contrast, the DNA cleavage activity of 1 was notably enhanced upon UV-irradiation (lambda(ex)=365 nm) followed by incubation. Under UV-irradiation, further DNA cleavage were occurred primary at 5'-G of GG steps within DNA. A DNA cleavage mechanism for 1, by which photo-induced one-electron oxidation of 5'-G of GG steps may occur along with ordinary alkylation, has been proposed.

MeSH terms

  • Alkylation
  • Animals
  • Anthraquinones / chemistry*
  • DNA / chemistry*
  • DNA / radiation effects
  • Male
  • Molecular Structure
  • Oxidation-Reduction
  • Photochemistry
  • Salmon
  • Spermatozoa / chemistry
  • Sulfones / chemistry*
  • Ultraviolet Rays

Substances

  • Anthraquinones
  • Sulfones
  • DNA