| Literature DB >> 31964062 |
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.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