Novel Bis-1,3,4-Thiadiazoles Derivatives: Synthesis, Spectroscopic Characterization, DFT Calculations and Evaluation of their Antimicrobial and Antioxidant Activities
Abstract
Keywords
Bis-thiadiazoles, Biological activity, DFT, IBSI, Force constant (FC).
References
- [1] Kaur P., Kaur R., Thiadiazole as an antimicrobial scaffold, Ann Trop Med & Public Health, 23 (2020) SP231542.
- [2] Szeliga M., Thiadiazole derivatives as anticancer agents, Pharmacological Reports, 72 (2020) 1079-1100.
- [3] Zhong X., Wang X., Chen L., Ruan X., Li Q., Zhang J., Chen Z., Xue W., Synthesis and biological activity of myricetin derivatives containing 1,3,4-thiadiazole scaffold, Chem. Cent. J., 11 (2017) 106.
- [4] Chudzik B., Bonio K., Dabrowski W., Pietrzak D., Niewiadomy A., Olender A., Pawlikowska-Pawlęga B., Gagoś M., Antifungal effects of a 1,3,4-thiadiazole derivative determined by cytochemical and vibrational spectroscopic studies, PLoS One, 14 (2019) 0222775.
- [5] Gautam A., Tyagi M., An insight into antitubercular activity associated with 1,3,4-thiadiazoles, Chemistry & Biology Interface, 10 (2020) 140-148.
- [6] Mayura K., Kirtee B., Biological potential of thiadiazole linked heterocycles: An overview, Journal of Current Pharma Research, 5 (2015)1578-1585.
- [7] Sharma B., Verma A., Prajapati S., Sharma U K., Synthetic methods, chemistry, and the anticonvulsant activity of thiadiazoles, Int. J Med. Chem, 2013 (2013) 348948.
- [8] Drapak I.V., Zimenkovsky B.S., Slabyy M.V., Holota S.M., Perekhoda L.O., Yaremkevych R.V., Nektegayev I.O., Synthesis and diuretic activity of novel 5-amino-1,3,4-thiadiazole-2-thiol derivatives, Biopolymers and Cell, 37 (2021) 33-45.
- [9] Parlak A.E., Koparır P., In vitro antioxidant properties of novel compound (1r, 2r) -1,2-bis- (5- (4-hydroxynaphthalen-1-ylazo) - [1,3,4] thiadiazol-2-yl) -ethane- 1,2-diole, Cumhuriyet Sci. J, 39-3 (2018) 658-667.
- [10] Madkour H.F., Azab M.E., Aly A.F., Khamees M.S.M., Novel heterocycles based on 1,3,4-Thiadiazole scaffold as insecticides, J. Environ. Sci., 40 (2017) 19-44.