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      Anticancer RuII and RhIII Piano-Stool Complexes that are Histone Deacetylase Inhibitors.

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          Abstract

          The first examples of RuII and RhIII piano-stool complex histone deacetylase (HDAC) inhibitors are presented. The novel complexes have antiproliferative activity against H460 non-small-cell lung carcinoma cells that is comparable to the clinically used HDAC inhibitor suberoylanilide hydroxamic acid (SAHA). Strong evidence for HDAC inhibition as a primary mechanism of action is provided. The complexes reported here represent an important step towards the design of highly active and selective HDAC inhibitors.

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          Author and article information

          Journal
          Chempluschem
          ChemPlusChem
          Wiley
          2192-6506
          2192-6506
          Dec 2016
          : 81
          : 12
          Affiliations
          [1 ] Department of Chemistry, Durham University, South Road, Durham, DH1 3LE, United Kingdom.
          [2 ] School of Biological and Biomedical Sciences, Durham University, South Road, Durham, DH1 3LE, United Kingdom.
          [3 ] School of Medicine, Pharmacy and Health, Durham University, Wolfson Research Institute, Queen's Campus, Stockton on Tees, TS17 6BH, United Kingdom.
          Article
          10.1002/cplu.201600413
          31964062
          f9ea9051-50ab-47d6-8097-ecc70e1f2db8
          © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
          History

          antitumour agents,bioorganometallic chemistry,histone deacetylase inhibitors,piano-stool complexes,ruthenium

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