Issue 1, 2012

Click JAHAs: conformationally restricted ferrocene-based histone deacetylase inhibitors

Abstract

A small library of ferrocene-based 1,2,3-triazole-containing hydroxamic acids has been synthesised employing click chemistry: 7-(4-ferrocenyl-1H-1,2,3-triazol-1-yl)-N-hydroxyheptanamide, 4b, containing the 1,2,3-triazole moiety adjacent to the ferrocene group, displayed excellent HDAC inhibition and activity in cells, inhibiting the deacetylation of tubulin as well as inducing cell cycle arrest.

Graphical abstract: Click JAHAs: conformationally restricted ferrocene -based histone deacetylase inhibitors

Supplementary files

Additions and corrections

Article information

Article type
Concise Article
Submitted
06 Aug 2011
Accepted
28 Sep 2011
First published
20 Oct 2011

Med. Chem. Commun., 2012,3, 61-64

Click JAHAs: conformationally restricted ferrocene-based histone deacetylase inhibitors

J. Spencer, J. Amin, R. Boddiboyena, G. Packham, B. E. Cavell, S. S. Syed Alwi, R. M. Paranal, T. D. Heightman, M. Wang, B. Marsden, P. Coxhead, M. Guille, G. J. Tizzard, S. J. Coles and J. E. Bradner., Med. Chem. Commun., 2012, 3, 61 DOI: 10.1039/C1MD00203A

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