Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1396914 | European Journal of Medicinal Chemistry | 2008 | 13 Pages |
Abstract
Novel imidazo[1,2-a]naphthyridinic systems 6a–15a and 6b–15b were obtained from Friedländer's reaction in imidazo[1,2-a]pyridine series. Most of the compounds were evaluated for their antitumor activity in the NCIs in vitro human tumor cell line screening panel. Among them, pentacyclic derivatives 13b and 14a exhibited in vitro activity comparable to anticancer agent such as amsacrine. Their mechanism of cytotoxicity action was unrelated to poisoning or inhibiting abilities against topo1. On the contrary, we highlighted a direct intercalation of the drugs into DNA by electrophoresis on agarose gel.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Mounir Andaloussi, Emmanuel Moreau, Nicolas Masurier, Jacques Lacroix, René C. Gaudreault, Jean-Michel Chezal, Anas El Laghdach, Damien Canitrot, Eric Debiton, Jean-Claude Teulade, Olivier Chavignon,