Biological activity of 3-chloro-azetidin-2-one derivatives having interesting antiproliferative activity on human breast cancer cell lines |
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Authors: | Adele Chimento Marina Sala Isabel M. Gomez-Monterrey Simona Musella Alessia Bertamino Anna Caruso Maria Stefania Sinicropi Rosa Sirianni Francesco Puoci Ortensia Ilaria Parisi Carmela Campana Emilia Martire Ettore Novellino Carmela Saturnino Pietro Campiglia Vincenzo Pezzi |
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Affiliation: | 1. Department of Pharmacy, Health and Nutrition Sciences, University of Calabria, 87036 Arcavacata di Rende, Cosenza, Italy;2. Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, Salerno, Italy;3. Department of Pharmaceutical and Toxicological Chemistry, University of Naples ‘Federico II’, 8013 Napoli, Italy;4. Department Pharmaco-Biological, University of Messina, 98168 Messina, Italy |
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Abstract: | Resveratrol (3,4′,5 tri-hydroxystilbene), a natural plant polyphenol, has gained interest as a non-toxic agent capable of inducing tumor cell death in a variety of cancer types. However, therapeutic application of these beneficial effects remains very limited due to its short biological half-life, labile properties, rapid metabolism and elimination. Different studies were undertaken to obtain synthetic analogs of resveratrol with major bioavailability and anticancer activity. We have synthesized a series 3-chloro-azetidin-2-one derivatives, in which an azetidinone nucleus connects two aromatic rings. Aim of the present study was to investigate the effects of these new 3-chloro-azetidin-2-one resveratrol derivatives on human breast cancer cell lines proliferation. Our results indicate that some azetidin-based resveratrol derivatives may become new potent alternative tools for the treatment of human breast cancer. |
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Keywords: | Resveratrol analogs anticancer drugs 3-Chloro-azetidin-2-one derivatives Breast cancer MCF-7 SKBR3 |
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