Chalcones
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-81404-5_10-1
Reference140 articles.
1. Abu-Dief AM, Nassar IF, Elsayed WH. Magnetic NiFe2O4 nanoparticles: efficient, heterogeneous and reusable catalyst for synthesis of acetylferrocene chalcones and their anti-tumour activity. Appl Organomet Chem. 2016;30(11):917–23.
2. Alarcón J, Alderete J, Escobar C, et al. Aspergillus niger catalyzes the synthesis of flavonoids from chalcones. Biocatal Biotransform. 2013;31(4):160–7.
3. Alberton EH, Damazio RG, Cazarolli LH, et al. Influence of chalcone analogues on serum glucose levels in hyperglycemic rats. Chem Biol Interact. 2008;171:355–62. https://doi.org/10.1016/j.cbi.2007.11.001.
4. Ali M, Khan M, Zaman K, Wadood A, et al. Chalcones: as potent α-amylase enzyme inhibitors; synthesis, in vitro, and in silico studies. Med Chem. 2021;17(8):903–12. https://doi.org/10.2174/1573406416666200611103039.
5. Alia M, Ramos S, Mateos R, et al. New chalcones as antioxidants and nitric oxide production inhibitors. Free Radic Res. 2003;37(6):637–45.
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