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Title: | Synthesis, structural characterization and cell death-inducing effect of novel palladium(II) and platinum(II) saccharinate complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl) pyridine on cancer cells in vitro |
Authors: | Büyükgüngor, Orhan Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı. Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Anabilim Dalı. Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı. 0000-0002-2849-3332 0000-0003-3118-8061 0000-0002-6729-7908 0000-0002-2717-2430 Arı, Ferda Aztopal, Nazlıhan İçsel, Ceyda Yılmaz, Veysel T. Güney, Emel Ulukaya, Engin K-5792-2018 AAI-3342-2021 L-7238-2018 AAV-4886-2020 L-6687-2018 AAG-7012-2021 24376085300 55853882900 55551960400 7006269202 25027291500 6602927353 |
Keywords: | Biochemistry & molecular biology Pharmacology & pharmacy Chemistry Palladium(II) and platinum(II) complexes Cancer Cytotoxicity Apoptosis Dna-binding Metal-complexes Antitumor Apoptosis Fluorescent Assay |
Issue Date: | Nov-2013 |
Publisher: | Pergamon-Elsevier Science |
Citation: | Arı, F. vd. (2013). "Synthesis, structural characterization and cell death-inducing effect of novel palladium(II) and platinum(II) saccharinate complexes with 2-(hydroxymethyl)pyridine and 2-(2-hydroxyethyl) pyridine on cancer cells in vitro". Bioorganic and Medicinal Chemistry, 21(21), 6427-6434. |
Abstract: | Four palladium(II) and platinum(II) saccharinate (sac) complexes with 2-(hydroxymethyl) pyridine (2-hmpy) and 2-(2-hydroxyethyl) pyridine (2-hepy), namely trans-[Pd(2-hmpy)(2)(sac)(2)]center dot H2O (1), trans-[Pt(2-hmpy)(2)(sac)(2)]center dot 3H(2)O (2), trans-[Pd(2-hepy)(2)(sac)(2)] (3) and trans-[Pt(2-hepy)(2)(sac)(2)] (4), have been synthesized and characterized by elemental analysis, UV-vis, IR and NMR. Single crystal X-ray analysis reveals that the metal(II) ions in each complex are coordinated by two sac and two 2-hmpy or 2-hepy ligands with a trans arrangement. Anticancer effects of 1-4 were tested against four different cancer cell lines (A549 and PC3 for lung cancer, C6 for glioblastoma, and Hep3B for liver cancer). Cytotoxicity was first screened by the MTT assay and the results were further confirmed by the ATP assay. The mode of cell death was determined by both histological and biochemical methods. Among the metal complexes, complex 2 resulted in relatively stronger anti-growth effect in a dose-dependent manner (3.13-200 mu M), compared to the others, by inducing apoptosis. |
URI: | https://doi.org/10.1016/j.bmc.2013.08.050 https://www.sciencedirect.com/science/article/pii/S0968089613007530 http://hdl.handle.net/11452/29451 |
ISSN: | 0968-0896 1464-3391 |
Appears in Collections: | PubMed Scopus Web of Science |
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