Synthesis, characterization and cytotoxic activity of substituted benzyl iminoether Pt(II) complexes of the type cis- and trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-R}(2)] (R = Me, OMe, F). X-ray structure of trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-F}(2)] (Articolo in rivista)

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  • Synthesis, characterization and cytotoxic activity of substituted benzyl iminoether Pt(II) complexes of the type cis- and trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-R}(2)] (R = Me, OMe, F). X-ray structure of trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-F}(2)] (Articolo in rivista) (literal)
Anno
  • 2008-01-01T00:00:00+01:00 (literal)
Alternative label
  • Mazzega Sbovata S. 1, Bettio F.2, Marzano C. 2, Tassan A. 1,Mozzon M.1, Bertani R. 1, Benetollo F.3, Michelin R. A. 1 (2008)
    Synthesis, characterization and cytotoxic activity of substituted benzyl iminoether Pt(II) complexes of the type cis- and trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-R}(2)] (R = Me, OMe, F). X-ray structure of trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-F}(2)]
    in Journal of inorganic biochemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Mazzega Sbovata S. 1, Bettio F.2, Marzano C. 2, Tassan A. 1,Mozzon M.1, Bertani R. 1, Benetollo F.3, Michelin R. A. 1 (literal)
Pagina inizio
  • 882 (literal)
Pagina fine
  • 891 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 102 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1. Department of Chemical Processes of Engineering, University of Padova. 2. Department of Pharmaceutical Sciences, University of Padova. 3. ICIS – C.N.R., Padova (literal)
Titolo
  • Synthesis, characterization and cytotoxic activity of substituted benzyl iminoether Pt(II) complexes of the type cis- and trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-R}(2)] (R = Me, OMe, F). X-ray structure of trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-F}(2)] (literal)
Abstract
  • New substituted benzyl iminoether derivatives of the type cis- and trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-R}(2)] (R = Me (1a, 2a), OMe (3a, 4a), F (5a, 6a)) have been synthesized and characterized by elemental analyses, FT-IR spectroscopy and NMR techniques. The iminoether ligands are in the E configuration, which is stable in solution and in the solid state, as confirmed by the H-1 NMR data. Complex trans-[PtCl2{E-N(H)=C(OMe)CH2-C6H4-p-F}(2)] (6a) was also characterized by an X-ray diffraction study. Complexes 1 a-6a have been tested against a panel of human tumor cell lines in order to evaluate their cytotoxic activity. cis-Isomers were significant more potent than the corresponding trans-isomers against all tumor cell lines tested; moreover, complexes la and 5a showed IC50 values from about 2-fold to 6-fold lower than those exhibited by cisplatin, used as reference platinum anticancer drug. (C) 2007 Elsevier Inc. All rights reserved. (literal)
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