Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/26912
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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