Formaldehyde-induced DNA cross-link of indolizino[1,2-b]quinolines derived from the A-D rings of camptothecin

J Med Chem. 2002 Dec 19;45(26):5809-12. doi: 10.1021/jm020235g.

Abstract

Camptothecin consists of a lactone E ring adjacent to tetracyclic A-D rings of a planar chromophore, which are essential for topoisomerase I inhibition and DNA interaction. The A-D rings can be exploited to develop DNA-sequence-reading molecules. Indolizino[1,2-b]quinoline derivatives substituted with a piperidinoethyloxy side chain and an aminomethyl function on rings A and D, respectively, were synthesized, and their DNA binding and formaldehyde-mediated bonding properties were investigated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Camptothecin / analogs & derivatives*
  • Camptothecin / chemical synthesis*
  • Camptothecin / chemistry
  • Cross-Linking Reagents / chemical synthesis*
  • Cross-Linking Reagents / chemistry
  • DNA / chemistry*
  • DNA Footprinting
  • Deoxyribonuclease I / chemistry
  • Formaldehyde / chemistry*

Substances

  • Cross-Linking Reagents
  • Formaldehyde
  • DNA
  • Deoxyribonuclease I
  • Camptothecin