Background: 3-Cyanopyridine analogues are significant moieties with a variety of biological effects such as
antioxidant, antimicrobial, anti-inflammatory and cytotoxic agents. In addition, they could be applied in the treatment of several
Objective: Cyclo-addition of 3a-e derivatives with malononitrile yielded the corresponding 6-(4-((3-cyano-pyridinyl) amino) phenyl)-4-
Methods: Physical and spectral analyses were performed to demonstrate the proper structures of all incorporated analogues. The in vitro
antimicrobial activity of the preps derivatives was investigated by testing them with a panel of pathogenic strains of bacteria and fungi. Antituberculosis activity occurred against the Mycobacterium tuberculosis H37Rv strain. When looking at cytotoxic agents for four different cell
lines, researchers found that their activity was persuasive compared with that of standard antibiotics. In addition, the antioxidant activity of
the synthesized analogues was evaluated using the DPPH method.
Results and Discussions: The synthesized analogues were examined to determine their activity against the M. tuberculosis H37Rv strain.
Derivatives 2c, 2e, 3d and 3e had good inhibition. Further screening was done for the highest potency against M. tuberculosis to determine
the MICs. The antioxidant efficacy was evaluated via the DPPH technique matched with vitamin C as a positive control. The prospective
results showed that the derivatives did not display scavenging efficacies in comparison with the standard.
Conclusion: Some synthesized derivatives displayed good potency against bacterial activity and M. Tuberculosis. However, the antioxidant
performance of these derivatives did not display scavenging efficacies compared to vitamin C. The cytotoxic activity of the synthesized
derivatives were examined against various cell lines to display good cytotoxic activity in the order 4a-e > 2a-e > 3a-b.