Issue 8, 2016

Natural products and their derivatives as tRNA synthetase inhibitors and antimicrobial agents

Abstract

The tRNA synthetase enzymes are promising targets for development of therapeutic agents against infections by parasitic protozoans (e.g. malaria), fungi and yeast, as well as bacteria resistant to current antibiotics. These ubiquitous enzymes load a particular amino acid onto its cognate tRNA to form an aminoacyl tRNA in preparation for protein synthesis by the ribosome. Although tRNA synthetases for a given amino acid are often similar in different organisms, slight differences in their sequence and structure can permit highly selective interaction with inhibitors. Hence, these enzymes have been successful targets of anti-infective agents for decades. They can also act as anticancer agents by preventing protein synthesis in human cells. Many inhibitors have been isolated from nature or have designs inspired by natural products. This review lists known naturally derived aaRS inhibitors and particularly aims to highlight advances in our understanding of their application as antibacterial, anticancer and antimalarial therapeutics. Advances in structural understanding, overcoming resistance and increasing inhibitor efficacy will also be discussed.

Graphical abstract: Natural products and their derivatives as tRNA synthetase inhibitors and antimicrobial agents

Article information

Article type
Review Article
Submitted
20 May 2016
Accepted
29 Jun 2016
First published
14 Jul 2016

Med. Chem. Commun., 2016,7, 1535-1545

Natural products and their derivatives as tRNA synthetase inhibitors and antimicrobial agents

R. V. K. Cochrane, A. K. Norquay and J. C. Vederas, Med. Chem. Commun., 2016, 7, 1535 DOI: 10.1039/C6MD00274A

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