Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/11125
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dc.contributor.authorPetrović, Zorica-
dc.contributor.authorĐorović Jovanović, Jelena-
dc.contributor.authorSimijonović, Dušica-
dc.contributor.authorTrifunović, Srećko-
dc.contributor.authorPetrović, Vladimir-
dc.date.accessioned2021-04-20T17:33:41Z-
dc.date.available2021-04-20T17:33:41Z-
dc.date.issued2018-09-01-
dc.identifier.issn03666352-
dc.identifier.urihttps://scidar.kg.ac.rs/handle/123456789/11125-
dc.description.abstract© 2018, Institute of Chemistry, Slovak Academy of Sciences. N-Salicylidene and N-vanillidene anil Schiff bases SB-1–5 were evaluated for their iron-coordinating properties. For this purpose, reactions with Fe(III) chloride were performed. The obtained results showed that salicylaldehyde bases SB-1 and SB-2 are the best coordinating ligands among the investigated SBs. The corresponding complexes are obtained in good yield and investigated using UV–Vis spectrophotometry and IR spectroscopy. The inhibitory potential of SB-1–5 against iron-containing enzyme lipoxygenase (LOX) was also tested. Salicylidene bases exerted better activity then vanilliden. The cytotoxic in vitro activities against human breast carcinoma MDA-MB-231 and human colon carcinoma HCT-116 cell lines were determined. Based on these results, SB-1 and SB-2 can be considered as interesting compounds for further in vivo investigations.-
dc.relation.ispartofChemical Papers-
dc.titleIn vitro study of iron coordination properties, anti-inflammatory potential, and cytotoxic effects of N-salicylidene and N-vanillidene anil Schiff bases-
dc.typeArticle-
dc.identifier.doi10.1007/s11696-018-0419-5-
dc.identifier.scopus85050726703-
Appears in Collections:Faculty of Science, Kragujevac
Institute for Information Technologies, Kragujevac

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