| Literature DB >> 28866270 |
Daniel S Wenholz1, Ming Zeng1, Cong Ma2, Marcin Mielczarek1, Xiao Yang2, Mohan Bhadbhade1, David St C Black1, Peter J Lewis3, Renate Griffith4, Naresh Kumar5.
Abstract
Knoevenagel condensation was employed to generate a set of molecules potentially capable of inhibiting the RNA polymerase-σ70/σA interaction in bacteria. Synthesis was achieved via reactions between a variety of indole-7-carbaldehydes and rhodanine, N-allylrhodanine, barbituric acid or thiobarbituric acid. A library of structurally diverse compounds was examined by enzyme-linked immunosorbent assay (ELISA) to assess the inhibition of the targeted protein-protein interaction. Inhibition of bacterial growth was also evaluated using Bacillus subtilis and Escherichia coli cultures. The structure-activity relationship studies demonstrated the significance of particular structural features of the synthesized molecules for RNA polymerase-σ70/σA interaction inhibition and antibacterial activity. Docking was investigated as an in silico method for the further development of the compounds.Entities:
Keywords: Antibacterial activity; Bacterial transcription; Indole; RNA polymerase; Structure-activity relationship (SAR)
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Year: 2017 PMID: 28866270 DOI: 10.1016/j.bmcl.2017.08.036
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823