ISSN 2738-0971 | eISSN 2738-1013

Marija Aksić

Faculty of Sciences and Mathematics, University of Priština in Kosovska Mitrovica, Kosovska Mitrovica, Serbia

Articles

Open Access Original Scientific Paper

DETERMINATION OF POLYPHENOL AND FLAVONOID CONTENT AND ANTIOXIDANT ACTIVITY OF ETHANOLIC, CHLOROFORM AND ETHYL ACETATE EXTRACT OF THE PLANT SPECIES Thymus serpyllum L.

This research aimed to examine the phytochemical composition, content of polyphenols and flavonoids, and antioxidant capacity of ethanolic, ethyl acetate, and chloroform extract of the plant species Thymus serpyllum L. The extracts were tested for the presence of alkaloids, tannins, saponins, phenolic compounds, flavonoids, steroids, terpenoids, cardiotonic glycosides, and coumarins. The total content of polyphenols was determined spectrophotometrically with the Folin-Ciocalteu reagent, according to Singleton's method, while the total content of flavonoids was determined using the method with aluminum chloride. The highest contents of polyphenols and flavonoids were determined in ethanolic extracts, where the measured values ranged from 111.00 ± 0.26 to 288.00 ± 0.23 mg GAE/g of dry extract for polyphenols, and 65.80 ± 0.19 to 198.22 ± 0.34 mg RE/g dry extract for flavonoids. The antioxidant activity was determined by the DPPH (2,2-diphenyl-1-picrylhydrazyl) assay. The tested extracts show a good effect on DPPH radical inhibition, with the IC50 values ranging from 35.15 ± 0.33 to 398.27 ± 0.24 μg/ml, and the greatest ability of ethanolic extract to neutralize the DPPH radical. Qualitative phytochemical analysis of the extracts showed a wide spectrum of phytochemicals, where ethanol, as the most polar solvent, extracts almost all tested phytochemicals.

Open Access Original Scientific Paper

SYNTHESIS, COMPLETE ASSIGNMENT OF 1H- AND 13C-NMR SPECTRA AND ANTIOXIDANT ACTIVITY OF NEW AZINE DERIVATIVE BEARING COUMARIN MOIETY

In this research, the synthesis of a new azine derivative with coumarin moiety was performed in three reaction steps, starting from 4-hydroxycoumarin. The first step in synthesis was the acetylation of 4-hydroxycoumarin to yield 3-acetyl-4-hydroxycoumarin and then the obtained 3-acetyl-4-hydroxycoumarin was reacted with hydrazine hydrate and give a corresponding hydrazone. Condensation of the hydrazone with 4-ethoxy-3-methoxybenzaldehyde afforded the target compound 1-[1-(4-hydroxy-2-oxo-2H-chromen-3-yl)-ethylidene]-2-(4-etoxy-3-methoxybenzylidene)-hydrazine in a good yield. The resulting azine derivative is fully spectrally characterized, including complete assignment of 1H- and 13C-NMR spectra, as well as 2D NMR (1H-1H COSY, NOESY, HSQC and HMBC) spectra. The antioxidant activity of corresponding hydrazone and target compound was evaluated by DPPH method where hydrazone derivative displayed a significant and target azine good antioxidant activity, with IC50 (μM) values 11.69 and 216.60, respectively.