Synthesis and anti-proliferative activity of new biphenyle-benzylidenethiazolidine-2,4-dione bis-adducts containing various heterocyclic cores - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Letters in Drug Design and Discovery Année : 2014

Synthesis and anti-proliferative activity of new biphenyle-benzylidenethiazolidine-2,4-dione bis-adducts containing various heterocyclic cores

Résumé

In the course of our ongoing program dedicated to the synthesis of anti-proliferative compounds, we prepared new troglitazone derivatives bearing a biphenyle moiety. The chromane heterocycle was further replaced by imidazole and triazole derivatives. Many compounds exhibited fair to high activity towards various cancer cell lines. Among them, compound 17b reduced cell viability leading to only 22-34% viable cells in four cancer cell lines at 10 mu M, but unfortunately also led to a low (13%) cell viability of non-malignant primary cultured human hepatocytes at 200 mu M. Interestingly, compound 11b also reduced cell viability in colon and liver cancer cell lines (29% and 24% cell viability respectively at 10 mu M), but maintained a high cell viability of non-malignant hepatocytes (reaching 71% cell viability at 200 mu M), thus exhibiting a huge selectivity.
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hal-01094215 , version 1 (11-12-2014)

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Maxime Meyer, Sandra Kuntz, Isabelle Grillier-Vuissoz, Hélène Martin, Lysiane Richert, et al.. Synthesis and anti-proliferative activity of new biphenyle-benzylidenethiazolidine-2,4-dione bis-adducts containing various heterocyclic cores. Letters in Drug Design and Discovery, 2014, 11 (3), pp.256-264. ⟨10.2174/15701808113106660080⟩. ⟨hal-01094215⟩
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