In:
Current Topics in Medicinal Chemistry, Bentham Science Publishers Ltd., Vol. 20, No. 25 ( 2020-11-03), p. 2289-2299
Abstract:
1,2,3-triazoles are five-membered heterocyclic scaffold; their broad-spectrum
biological activities are known. Researchers around the world are increasingly being interested in this emerging area, owing to its immense pharmacological scope. Objective: This work summarizes the synthesis of 1,2,3-triazoles and the significance of this pattern as a
lead structure for new drug molecules discovery. Methods: 1,2,3-triazoles can be obtained on a multigram scale through “click chemistry” under ambient
conditions. Results: Sixteen compounds were synthesized and evaluated on five microbial strains E. coli, E. faecalis,
P. aeruginosa, S. aureus and C. albicans. NMR, MS and IR were used to characterize all compounds. They were evaluated with their Minimum Inhibitory Concentrations (MICs) and interesting results
were obtained with compounds 12a, 12b, 3, 2a and 2c, with MIC 0.14 μM (P. aeruginosa), 1.08 μM (E. coli), 1.20 μM (E. faecalis and C. albicans), 3.5 μM (E. faecalis) and 4.24 μM (C. albicans),
respectively. P. aeruginosa and C. albicans were the most sensitive among all the strains. Conclusion: The synthesized compounds were found as potential antimicrobial agents against Gram (+),
Gram (-) strains and fungi.
Type of Medium:
Online Resource
ISSN:
1568-0266
DOI:
10.2174/1568026620666200819143029
Language:
English
Publisher:
Bentham Science Publishers Ltd.
Publication Date:
2020
SSG:
15,3
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