Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/16051
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dc.contributor.authorBranković, Jovica-
dc.contributor.authorKrokidis M.-
dc.contributor.authorDousi I.-
dc.contributor.authorPapadopoulos, Kyriakos-
dc.contributor.authorPetrović, Zorica-
dc.contributor.authorPetrović, Vladimir-
dc.date.accessioned2023-02-08T16:22:32Z-
dc.date.available2023-02-08T16:22:32Z-
dc.date.issued2022-
dc.identifier.issn1381-1991-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/16051-
dc.description.abstractSelected salicylidene imines were evaluated for their antioxidant and cytotoxic potentials. Several of them exerted potent scavenging capacity towards ABTS radical and hydrogen peroxide. The insight into the preferable antioxidative mechanism was reached employing density functional theory. In the absence of free radicals, the SPLET mechanism is dominant in polar surroundings, while HAT is prevailing in a non-polar environment. The results obtained for the reactions of the most active compounds with some medically relevant radicals pointed out competition between HAT and SPLET mechanisms. The assessment of their cytotoxic properties revealed inhibition of ER-a human breast adenocarcinoma cells or estrogen-independent prostate cancer cells. Molecular docking study with the cyclooxygenase (COX) 2 enzyme was performed to examine the most probable bioactive conformations and possible interactions between the tested derivatives and COX-2 binding pocket. Graphical abstract: [Figure not available: see fulltext.]-
dc.rightsinfo:eu-repo/semantics/restrictedAccess-
dc.sourceMolecular Diversity-
dc.titleAntioxidant and cytotoxic activities of selected salicylidene imines: experimental and computational study-
dc.typearticle-
dc.identifier.doi10.1007/s11030-021-10370-9-
dc.identifier.scopus2-s2.0-85124550814-
Appears in Collections:Faculty of Science, Kragujevac

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