Synthesis and cytostatic properties of some 6H-Indolo[2, 3-b][1, 8]naphthyridine derivatives

Arch Pharm (Weinheim). 2004 Aug;337(8):434-9. doi: 10.1002/ardp.200200696.

Abstract

The new and efficient synthesis of the title heterocyclic ring system is described starting from suitable 2-chloro-1, 8-naphthyridines. The synthesized 6H-indolo[2, 3-b][1, 8]naphthyridine derivatives were tested in vitro on 55 tumor cell lines for their anticancer properties. The presence of the acetylamino moiety at position 3 in the main ring system proved to be crucial for the cytostatic activity of this class of compounds.

MeSH terms

  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Cell Division / drug effects
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Humans
  • Indicators and Reagents
  • Indoles / chemical synthesis*
  • Indoles / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Naphthyridines / chemical synthesis*
  • Naphthyridines / pharmacology*
  • Structure-Activity Relationship

Substances

  • 6H-indolo(2, 3-b)(1, 8)naphthyridine
  • Antineoplastic Agents
  • Indicators and Reagents
  • Indoles
  • Naphthyridines