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Synthesis and biological evaluation of triazolylnucleosides as antibacterial and anticancer agents
Journal article   Peer reviewed

Synthesis and biological evaluation of triazolylnucleosides as antibacterial and anticancer agents

. Ankit, T. Wang, R.N. Veedu, F. Abdmouleh, M.E. Arbi and S. Kumar
Chemical Data Collections, Vol.28, Art.100429
2020
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Abstract

A series of novel triazolylnucleosides has been efficiently synthesized (6a-h, 7a-b) by azide–alkyne 1,3-dipolar cycloaddition reaction and evaluated for antibacterial and anticancer activities. These nucleosides (6a-h) were screened against Staphylococcus aureus (ATCC 6538), gram-positive and Escherichia coli (ATCC 10536), Salmonella and Pseudomonas gram-negative bacterial strains. Among the series, three compounds (6c-e) exhibited significant levels of antibacterial activity against Staphylococcus aureus in reference to the standard drug, Levofloxacin. Triazolylnucleosides (6a-h) were also screened for anti-proliferative activities against cancer cell lines such as Huh-7 liver cancer cells. Three compounds (6e, 7a-b) have displayed promising anti-proliferative activity against Huh-7 and U87G cancer cells lines.

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