Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/19790
Title: Synthesis, structural characterization, cytotoxic properties and DNA binding of a dinuclear copper(II) complex
Author: Leite Ferreira, B. J. M.
Brandao, P.
Meireles, M.
Martel, Fátima
Correia-Branco, Ana
Fernandes, Diana M.
Santos, T. M.
Felix, V.
Keywords: PI-PI STACKING
CRYSTAL-STRUCTURE
ANTICANCER ACTIVITY
MAGNETIC-PROPERTIES
NUCLEASE ACTIVITY
CU(II) COMPLEXES
1,10-PHENANTHROLINE COPPER
PLATINUM COMPLEXES
ANTITUMOR-ACTIVITY
METAL-COMPLEXES
Issue Date: 2016
Publisher: ELSEVIER SCIENCE INC
Abstract: In this study a novel dinuclear copper(II) complex with adenine and phenanthroline has been synthesized and its structure determined by single crystal X-ray diffraction. In the dinuclear complex [Cu-2(mu-adenine)(2)(phen)(2)(H2O)2](NO3)(4)center dot 0.5H(2)O (phen = 1,10-phenanthroline) (1) the two Cu(II) centres exhibit a distorted square pyramidal coordination geometry linked by two nitrogen donors from adenine bridges leading to a Cu-Cu distance of 3.242(3) angstrom. Intramolecular and intermolecular pi center dot center dot center dot pi interactions as well as an H-bonding network were observed. The antitumor capacity of the complex has been tested in vitro against human cancer cell lines, cervical carcinoma (HeLa) and colorectal adenocarcinoma (Caco-2), by metabolic tests, using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide as reagent. The complex 1 has remarkable low IC50 values of 0.87 +/- 0.06 mu M (HeLa) and 0.44 +/- 0.06 mu M (Caco-2), when compared with values for cisplatin against the same cell lines. The interaction of complex 1 with calf thymus DNA (CT DNA) was further investigated by absorption and fluorescence spectroscopic methods. A binding constant of 5.09 x 10(5) M-1 was obtained from UV-vis absorption studies. (C) 2016 Elsevier Inc. All rights reserved.
Peer review: yes
URI: http://hdl.handle.net/10773/19790
DOI: 10.1016/j.jinorgbio.2016.04.026
ISSN: 0162-0134
Publisher Version: 10.1016/j.jinorgbio.2016.04.026
Appears in Collections:CICECO - Artigos



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