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Title: | New water-soluble copper (II) complexes including 4,7-dimethyl-1,10-phenanthroline and l-tyrosine: Synthesis, characterization, DNA interactions and cytotoxicities |
Authors: | Zorlu, Yunus Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Biyoloji Anabilim Dalı. Uludağ Üniversitesi/Fen-Edebiyat Fakültesi/Kimya Anabilim Dalı. 0000-0002-0026-7755 0000-0002-3595-6286 0000-0002-7687-3284 0000-0002-0483-9642 İnci, Duygu Aydın, Rahmiye Yılmaz, Dilek Gençkal, Hasene Mutlu Vatan, Özgür Çinkiliç, Nilüfer AAH-2888-2021 AAH-5296-2021 O-7508-2015 AAH-8936-2021 G-2201-2019 55082306300 56261495600 6701369462 57212275330 16235098100 26533892300 |
Keywords: | 4,7-Dimethyl-1,10-phenanthroline Copper(II) Cytotoxicity DNA binding and cleavage l-tyrosine Single crystal X-ray diffraction Mixed-ligand complexes Crystal-structure Weak-interactions Ruthenium(II) complexes Binding properties Cleavage Photocleavage 1,10-phenanthroline Fluorescence Stabilities Spectroscopy Amino acids Binding energy Complexation Copper Cytotoxicity DNA Electrophoresis Emission spectroscopy Nuclear magnetic resonance spectroscopy Platinum compounds Single crystals Synthesis (chemical) Thermoanalysis X ray diffraction 4,7-Dimethyl-1,10-phenanthroline Agarose gel electrophoresis DNA binding and cleavages DNA-binding properties l-Tyrosine Single crystal x-ray diffraction Thermal denaturations Water-soluble copper Copper compounds |
Issue Date: | 5-Feb-2015 |
Publisher: | Pergamon-Elsevier |
Citation: | İnci, D. vd. (2015). "New water-soluble copper (II) complexes including 4,7-dimethyl-1,10-phenanthroline and l-tyrosine: Synthesis, characterization, DNA interactions and cytotoxicities". Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy, 136 (Part B), 761-770. |
Abstract: | Two new water-soluble copper(II) complexes, [Cu(dmphen)(2)(NO3)]NO3 (1), [Cu(dmphen)(tyr)(H2O)] NO3 center dot H2O (2) and the diquartemary salt of dmphen (dmphen = 4,7-dimethyl-1,10-phenanthroline and tyr = L-tyrosine), have been synthesized and characterized by elemental analysis, H-1 NMR, C-13 NMR and IR spectroscopy, thermal analysis and single crystal X-ray diffraction techniques. The CT-DNA binding properties of these compounds have been investigated by absorption, emission spectroscopy and thermal denaturation measurements. The supercoiled pBR322 plasmid DNA cleavage activity of these compounds has been explored by agarose gel electrophoresis. The cytotoxicity of these compounds against MCF-7, Caco-2, A549 cancer cells and BEAS-2B healthy cells was also studied by the XTT method. Complexes 1 and 2 exhibit significant cytotoxicity, with lower IC50 values than those of cisplatin. |
URI: | https://doi.org/10.1016/j.saa.2014.09.093 https://www.sciencedirect.com/science/article/pii/S1386142514014516 http://hdl.handle.net/11452/26912 |
ISSN: | 1386-1425 |
Appears in Collections: | Scopus Web of Science |
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