Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/319260
Type: Artigo de periódico
Title: New Antibacterial Agents: Hybrid Bioisoster Derivatives As Potential E. Coli Fabh Inhibitors
Abstract: The development of resistance to antibiotics by microorganisms is a major problem for the treatment of bacterial infections worldwide, and therefore, it is imperative to study new scaffolds that are potentially useful in the development of new antibiotics. In this regard, we propose the design, synthesis and biological evaluation of hybrid sulfonylhydrazone bioisosters/furoxans with potential antibacterial (Escherichia coli) activity. The most active compound of the series, (E)-3-methyl-4-((2-tosylhydrazono)methyl)-1,2,5-oxadiazole 2-oxide, with a MIC = 0.36 μM, was not cytotoxic when tested on Vero cells (IC50 >100 μM). To complement the in vitro screening, we also studied the interaction of the test compounds with β-ketoacyl acyl carrier protein synthase (FabH), the target for the parent compounds, and we observed three important hydrogen-bonding interactions with two important active site residues in the catalytic site of the enzyme, providing complementary evidence to support the target of the new hybrid molecules. © 2016 Elsevier Ltd
Editor: Elsevier Ltd
Citation: Bioorganic And Medicinal Chemistry Letters. Elsevier Ltd, v. 26, p. 3988 - 3993, 2016.
Rights: fechado
Identifier DOI: 10.1016/j.bmcl.2016.06.089
Address: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979539452&partnerID=40&md5=5a6d18290931c69be5ec39c8a0651733
Date Issue: 2016
Appears in Collections:Unicamp - Artigos e Outros Documentos

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