Activity of rat cytosolic thioredoxin reductase is strongly decreased by (Articolo in rivista)

Type
Label
  • Activity of rat cytosolic thioredoxin reductase is strongly decreased by (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Alternative label
  • Mura P, Camalli M, Bindoli A, Sorrentino F, Casini A, Gabbiani C, Corsini M, (2007)
    Activity of rat cytosolic thioredoxin reductase is strongly decreased by
    in Journal of medicinal chemistry
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Mura P, Camalli M, Bindoli A, Sorrentino F, Casini A, Gabbiani C, Corsini M, (literal)
Pagina inizio
  • 5871 (literal)
Pagina fine
  • 5874 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 50 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Institute of Crystallography, Area della Ricerca di Roma 1 (CNR), Via Salaria Km 29,300, Montelibretti, Rome, Italy, Istituto di Neuroscienze (CNR), Sezione di PadoVa c/o Dipartimento di Chimica Biologica, PadoVa, Italy, Dipartimento di Chimica Biologica, UniVersita` degli Studi di PadoVa, Viale G. Colombo 3, 35121 PadoVa, Italy, Department of Chemistry, UniVersity of Siena, Via De Gasperi 2, I-53100 Siena, Italy, and Department of Chemistry, UniVersity of Florence, Via della Lastruccia 3, 50019 Sesto Fiorentino, Firenze, Italy (literal)
Titolo
  • Activity of rat cytosolic thioredoxin reductase is strongly decreased by (literal)
Abstract
  • A novel \"Keppler type\" ruthenium(III) compound trans- [bis(2-amino 5-methylthiazole)tetrachlororuthenate(III)] 1, of potential interest as an anticancer agent, was designed, synthesized, and characterized. Its interactions with various proteins were analyzed, including the selenoenzyme thioredoxin reductase, an emerging target for anticancer metallodrugs. The selective inhibition of the cytosolic form of this selenoenzyme was documented, this being the first report of significant thioredoxin reductase inhibition by a ruthenium compound. (literal)
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