Synthesis and evaluation of antibacterial and antioxidant activity of novel 2-phenyl-quinoline analogs derivatized at position 4 with aromatically substituted 4<i>H</i>-1,2,4-triazoles release_dsncwyni6rcuhgmtmvo3djsny4

by Donatella Verbanac, Ritu Malik, Mahesh Chand, Khushbu Kushwaha, Monika Vashist, Mario Matijašić, Višnja Stepanić, Mihaela Perić, Hana Čipčić Paljetak, Luciano Saso, Subhash C. Jain

Published by Figshare.

2016  

Abstract

A set of novel quinolone–triazole conjugates (<b>12</b>–<b>31</b>) were synthesized in three steps in good yields starting from 2-phenylquinoline-4-carboxylic acid. All the intermediates, as well as the final 1,2,4-triazolyl quinolines were fully characterized by their detailed spectral analysis utilizing different techniques such as IR, <sup>1</sup>H NMR, <sup>13</sup>C NMR, and finally mass spectrometry. All the synthesized compounds were evaluated <i>in vitro</i> for their potential antibacterial activity and their preliminary safety profile was assessed through cytotoxicity assay. Additionally, six selected conjugates were evaluated for their antioxidative properties on the basis of density functional theory calculations, using radical scavenging assay (DPPH) and cellular antioxidant assay. The reported results encourage further investigation of selected compounds and are shading light on their potential pharmacological use.
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