Synthesis, Characterization, Antioxidant, Antibacterial and Enzyme Inhibitor Evaluation of New Furan-Tethered 1,3,4-Thiadiazoles
Halit Muglu1, Mohamed Ab. Khalifa Ibrahim1, Hasan Yakan2*, Omer Tas3, Gurkan Bilir3, Ercument Aksakal4, Temel Kan Bakir1, Ergin Murat Altuner5, Murat Senturk6, Deniz Ekici3*
Novel furan-tethered 1,3,4-thiadiazoles (1-5) were prepared and characterized by FT-IR, 1H NMR, 13C NMR and elemental analysis. Compounds, in general, showed antibacterial effects on selected bacteria, including K. pneumoniae, E. faecium, S. epidermidis, S. macrescens, B. subtilis, E. coli, and S. kentucky. Besides, none of the compounds had effects on P. aeruginosa. In vitro antioxidant activity determination was carried out using the DPPH method, and results of the synthesized compounds were found to be close to each other showing lower antioxidant activity than the standard used (ascorbic acid). In vitro acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition of the synthesized compounds was performed using Ellman's spectrophotometry method. The compounds showed inhibition with IC50 values ranging from 27.39 to 45.71 µM for AChE and 13.35 to 115.17 µM for BChE. Among the synthesized derivatives, compound 2 exhibited the strongest inhibitory effect against both AChE, and BChE.
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