Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.21/2148
Título: DNA interaction and cytotoxicity studies of new ruthenium(II) cyclopentadienyl derivative complexescontaining heteroaromatic ligands
Autor: Moreno, Virtudes
Font-Bardia, Merce
Calvet, Teresa
Lorenzo, Júlia
Aviles, Francesc X.
Garcia, M. Helena
Morais, Tânia S.
Valente, Andreia
Robalo, M. Paula
Palavras-chave: Ruthenium (II)
Cyclopentadienyl derivatives
X-ray structures
Antiproliferative assays
In-Vitro cytotoxicity
Cancer-cell-growth
Nami-A
Arene complexes
Crystal-structure
Chemistry
Inhibition
Proliferation
Expression
Assay
Data: Fev-2011
Editora: Elsevier Science INC
Citação: MORENO, Virtudes; FONT-BARDIA, Merce; CALVET, Teresa; LORENZO, Júlia; AVILES, Francesc X.; GARCIA, M. Helena; MORAIS, Tânia S.; VALENTE, Andreia; ROBALO, M. Paula - DNA interaction and cytotoxicity studies of new ruthenium(II) cyclopentadienyl derivative complexescontaining heteroaromatic ligands. Journal of Inorganic Biochemistry. ISSN 0162-0134. Vol. 105, n.º2 (2011) p. 241-249.
Resumo: Four ruthenium(II) complexes with the formula [Ru(eta(5)-C(5)H(5))(PP)L][CF(3)SO(3)], being (PP = two triphenylphosphine molecules), L = 1-benzylimidazole, 1; (PP = two triphenylphosphine molecules), L = 2,2'bipyridine, 2; (PP = two triphenylphosphine molecules), L = 4-Methylpyridine, 3; (PP = 1,2-bis(diphenylphosphine) ethane), L = 4-Methylpyridine, 4, were prepared, in view to evaluate their potentialities as antitumor agents. The compounds were completely characterized by NMR spectroscopy and their crystal and molecular structures were determined by X-ray diffraction. Electrochemical studies were carried out giving for all the compounds quasi-reversible processes. The images obtained by atomic force microscopy (AFM) suggest interaction with pBR322 plasmid DNA. Measurements of the viscosity of solutions of free DNA and DNA incubated with different concentrations of the compounds confirmed this interaction. The cytotoxicity of compounds 1234 was much higher than that of cisplatin against human leukemia cancer cells (HL-60 cells). IC(50) values for all the compounds are in the range of submicromolar amounts. Apoptotic death percentage was also studied resulting similar than that of cisplatin. (C) 2010 Elsevier Inc. All rights reserved.
Peer review: yes
URI: http://hdl.handle.net/10400.21/2148
ISSN: 0162-0134
Aparece nas colecções:ISEL - Eng. Quim. Biol. - Artigos



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