Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591036 | Bioorganic & Medicinal Chemistry Letters | 2014 | 8 Pages |
Abstract
New benzothieno[3,2-d]-1,2,3-triazines, together with precursors triazenylbenzo[b]thiophenes, were designed, synthesized and screened as anticancer agents. The structural features of these compounds prompted us to investigate their DNA binding capability through UV-vis absorption titrations, circular dichroism, and viscometry, pointing out the occurrence of groove-binding. The derivative 3-(4-methoxy-phenyl)benzothieno[3,2-d]-1,2,3-triazin-4(3H)-one showed the highest antiproliferative effect against HeLa cells and was also tested in cell cycle perturbation experiments. The obtained results assessed for the first time the anticancer activity of benzothieno[3,2-d]-1,2,3-triazine nucleus, and we related it to its DNA-binding properties.
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Authors
Antonino Lauria, Alessia Alfio, Riccardo Bonsignore, Carla Gentile, Annamaria Martorana, Giuseppe Gennaro, Giampaolo Barone, Alessio Terenzi, Anna Maria Almerico,