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Targeting methionyl tRNA synthetase: design, synthesis and antibacterial activity against Clostridium difficile of novel 3-biaryl-Nbenzylpropan- 1-amine derivatives

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Author
Eissa, Ahmed
Blaxland, James
Williams, Rhodri
Metwally, Kamel
El-Adl, Sobhy
Lashine, El-Sayed
Baillie, Leslie
Simons, Claire
Date
2016-02-22
Acceptance date
2016-01-05
Type
Article
Publisher
Taylor and Francis
ISSN
1475-6374
Metadata
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Abstract
The synthesis of a series of benzimidazole-N-benzylpropan-1-amines and adenine-N-benzylpropan-1-amines is described. Subsequent evaluation against two strains of the anaerobic bacterium Clostridium difficile was performed with three amine derivatives displaying MIC values of 16 μg/mL. Molecular docking studies of the described amines determined that the amines interact within two active site pockets of C. difficile methionyl tRNA synthetase with methoxy substituents in the benzyl ring and an adenine biaryl moiety resulting in optimal binding interactions.
Journal/conference proceeding
Journal of Enzyme Inhibition and Medicinal Chemistry;
Citation
Eissa, A.G., Blaxland, J.A., Williams, R.O., Metwally, K.A., El-Adl, S.M., Lashine, E.S.M., Baillie, L.W. and Simons, C. (2016) 'Targeting methionyl tRNA synthetase: design, synthesis and antibacterial activity against Clostridium difficile of novel 3-biaryl-N-benzylpropan-1-amine derivatives. Journal of enzyme inhibition and medicinal chemistry', 31(6), pp.1694-1697. DOI: 10.3109/14756366.2016.1140754.
URI
http://hdl.handle.net/10369/10418
DOI
https://doi.org/10.3109/14756366.2016.1140754
Description
Article published in Journal of Enzyme Inhibition and Medicinal Chemistry on 22 February 2016, available open access at: https://doi.org/10.3109/14756366.2016.1140754.
Rights
https://creativecommons.org/licenses/by/4.0/
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