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Issue 1, 2014

2-Hydroxy-substituted cinnamic acids and acetanilides are selective growth inhibitors of Mycobacterium tuberculosis

Author affiliations

Abstract

Selective chemical hits are required for feeding the initial discovery phase of the anti-tuberculosis therapeutics pipeline. These chemical entities should ideally target novel mechanisms of action in order to tackle drug resistance in Mycobacterium tuberculosis. In this work, hydroxycinnamic acid and acetamidophenol skeleta were employed for assessing the effects of constitutional isomerism on in vitro anti-TB activity. The whole cell evaluation of minimum inhibitory concentration values of different substituted cinnamic acids and acetamidophenols showed that the free ortho hydroxyl group conferred both potency and selectivity. Both 2-coumaric acid and 2-acetamidophenol showed minimum inhibitory concentration below 150 μM against M. tuberculosis H37Rv and selectivity index higher than 30.

Graphical abstract: 2-Hydroxy-substituted cinnamic acids and acetanilides are selective growth inhibitors of Mycobacterium tuberculosis

Supplementary files

Article information


Submitted
03 Sep 2013
Accepted
27 Oct 2013
First published
11 Nov 2013

Med. Chem. Commun., 2014,5, 47-50
Article type
Concise Article

2-Hydroxy-substituted cinnamic acids and acetanilides are selective growth inhibitors of Mycobacterium tuberculosis

J. D. Guzman, P. N. Mortazavi, T. Munshi, D. Evangelopoulos, T. D. McHugh, S. Gibbons, J. Malkinson and S. Bhakta, Med. Chem. Commun., 2014, 5, 47 DOI: 10.1039/C3MD00251A

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