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Назив: New water-soluble ruthenium(II) terpyridine complexes for anticancer activity: Synthesis, characterization, activation kinetics, and interaction with guanine derivatives
Аутори: Rilak, Ana
Bratsos, Ioannis
zangrando, ennio
Kljun J.
Turel, Iztok
Bugarčić Z.
Alessio, Enzo
Датум издавања: 2014
Сажетак: With the aim of assessing whether ruthenium(II) compounds with meridional geometry might be utilized as potential antitumor agents, a series of new, water-soluble, monofunctional ruthenium(II) complexes of the general formula mer-[Ru(L3)(N-N)X][Y]n (where L3 = 2,2′:6′,2″-terpyridine (tpy) or 4′-chloro-2,2′: 6′,2″-terpyridine (Cl-tpy), N-N = 1,2-diaminoethane (en), 1,2-diaminocyclohexane (dach), or 2,2′-bipyridine (bpy); X = Cl or dmso-S; Y = Cl, PF6, or CF3SO3; n = 1 or 2, depending on the nature of X) were synthesized. All complexes were fully characterized by elemental analysis and spectroscopic techniques (IR, UV/visible, and 1D and 2D NMR), and for three of them, i.e., [Ru(Cl-tpy)(bpy)Cl][Cl] (3Cl), [Ru(Cl-tpy)(en)(dmso-S)][Y]2 [Y = PF6 (6PF6), CF3SO3 (6OTf)] and [Ru(Cl-tpy)(bpy)(dmso-S)] [CF3SO3]2 (8OTf), the X-ray structure was also determined. The new terpyridine complexes, with the exception of 8, are well soluble in water (>25 mg/mL). 1H and 31P NMR spectroscopy studies performed on the three selected complexes [Ru(Cl-tpy)(N-N)Cl]+ [N-N = en (1), dach (2), and bpy (3)] demonstrated that, after hydrolysis of the Cl ligand, they are capable of interacting with guanine derivatives [i.e., 9-methylguanine (9MeG) or guanosine-5′-monophosphate (5′-GMP)] through N7, forming monofunctional adducts with rates and extents that depend strongly on the nature of N-N: 1 ≈ 2 ≫ 3. In addition, compound 1 shows high selectivity toward 5′-GMP compared to adenosine-5′-monophosphate (5′-AMP), in a competition experiment. Quantitative kinetic investigations on 1 and 2 were performed by means of UV/visible spectroscopy. Overall, the complexes with bidentate aliphatic diamines proved to be superior to those with bpy in terms of solubility and reactivity (i.e., release of Cl- and capability to bind guanine derivatives). Contrary to the chlorido compounds, the corresponding dmso derivatives proved to be inert (viz., they do not release the monodentate ligand) in aqueous media. © 2014 American Chemical Society.
URI: https://scidar.kg.ac.rs/handle/123456789/12268
Тип: article
DOI: 10.1021/ic5005215
ISSN: 0020-1669
SCOPUS: 2-s2.0-84902494164
Налази се у колекцијама:Institute for Information Technologies, Kragujevac

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