Antioxidant Activities of Some New Chromonyl-2,4-Thiazolidinediones and Chromonyl-2,4-Imidazolidinediones Having Chromone Cores |
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Authors: | Paweł Berczyński Aleksandra Kładna Irena Kruk Teresa Piechowska Hassan Y. Aboul-Enein Oya Bozdağ-Dündar Meltem Ceylan-Unlusoy |
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Affiliation: | 1. Szczecin Institute of Physics, West Pomeranian University of Technology, al. Piastów 48, 70-311, Szczecin, Poland 2. Department of History of Medicine and Medical Ethics, Pomeranian Medical University, Rybacka 1, 70-204, Szczecin, Poland 3. Pharmaceutical and Medicinal Chemistry Department, Pharmaceutical and Drug Industries Research Division, National Research Centre, Dokki, Cairo, 12311, Egypt 4. Faculty of Pharmacy, Department of Pharmaceutical Chemistry, Ankara University, 06100 Tando?an, Ankara, Turkey
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Abstract: | The antioxidant properties of 11 new synthesized chromonyl-2,4-thiazolidinediones and chromonyl-2,4-imidazolidinediones (CBs) were investigated. The antioxidant activities and mechanisms of the CBs interaction with reactive oxygen species (ROS) were clarified using various in vitro antioxidant assay methods including superoxide anion radical ( $ mathrm{O}overline{{}_2^{bullet }} $ ), hydroxyl radical (HO?), 1,1-diphenyl-2-picryl-hydrazyl free radical (DPPH?) scavenging activity and the iron (II)-ferrozine complex formation. The potassium superoxide/18-crown-6 ether dissolved in dimethylsulfoxide (DMSO) was applied as a source of superoxide anion radical. Hydroxyl radicals were produced in the Fenton-like reaction Fe(II)+H2O2. Chemiluminescence, spectrophotometry, and electron paramagnetic resonance (EPR) spectroscopy using 5,5-dimethyl-1-pyrroline-1-oxide (DMPO) as spin trap were applied as the measurement techniques. The CBs examined that exhibited good free radical scavenging activity also showed strong total antioxidant power capacity. Possible mechanisms of antioxidation are proposed to explain the differences in the experimental results between the chromone derivatives with imidazolidine-2,4-dione ring and those with thiazolidine-2,4-dione ring. In conclusion, some of the new CBs are promising to be applied as inhibitors of free radicals. |
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