Literature DB >> 31964062

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

Jasmine M Cross1, Tim R Blower2, Natalie Gallagher3, Jason H Gill3, Kimberly L Rockley3, James W Walton1.   

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.
© 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

Entities:  

Keywords:  antitumour agents; bioorganometallic chemistry; histone deacetylase inhibitors; piano-stool complexes; ruthenium

Year:  2016        PMID: 31964062     DOI: 10.1002/cplu.201600413

Source DB:  PubMed          Journal:  Chempluschem        ISSN: 2192-6506            Impact factor:   2.863


  2 in total

1.  Anticancer Ruthenium Complexes with HDAC Isoform Selectivity.

Authors:  Jasmine M Cross; Tim R Blower; Alexander D H Kingdon; Robert Pal; David M Picton; James W Walton
Journal:  Molecules       Date:  2020-05-21       Impact factor: 4.411

2.  Bioactive Salen-type Schiff Base Transition Metal Complexes as Possible Anticancer Agents.

Authors:  Maryam Damercheli; Mahdi Mahdi; Bita Mehravi; Mehdi Shafiee Ardestani
Journal:  Iran J Pharm Res       Date:  2019       Impact factor: 1.696

  2 in total

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