Phytochemical Composition, Antioxidant, Antiacetylcholinesterase, and Cytotoxic Activities of L.

Int J Anal Chem

Laboratoire de Chimie Analytique et Électrochimie, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, Tunis 2092, Tunisia.

Published: July 2021

L. () is regarded as an aromatic plant. It was used for its excellent biological properties in traditional medicine. The aerial part was extracted successively by maceration with three solvents increasing polarity (cyclohexane (CYH), dichloromethane (DCM), and methanol (MeOH)) to evaluate their chemical compositions and biological activities. The extracts were rich in phenolic compounds (13.0 to 249.8 mg GAE/g of dry weight (dw)). The MeOH extract has presented remarkable IC = 6.2 g/mL for anti-DPPH and 31.6 g/mL for anti-AChE. However, the DCM extract has the highest cytotoxic activity against the two cancer cells (HCT-116 and MCF-7) (69.2 and 77.2% inhibition at 50 g/mL, respectively). Interestingly, GC-MS analysis enabled to identify three new compounds in extracts, such as L-(-)-arabitol (5), D-(-) fructopyranose (7) detected only in MeOH extract, and 2, 5-dihydroxyacetophenone (3) detected in all extracts. For HPLC chromatograms, cardamonin (8), 5-hydroxy-3'-methoxyflavone (17), and 3'-hydroxy-b-naphthoflavone (18) showed the highest concentrations of 74.0, 55.5, and 50.4 mg/g of dw, respectively, among others who are identified. Some phenolic compounds were identified and quantified by HPLC in more than one organic extract, such as 4', 5-dihydroxy-7-methoxyflavone (13), 4', 5-dihydroxy-7-methoxyflavone (14), 5-hydroxy-3'-methoxyflavone (17), and 3'-hydroxy-b-naphthoflavone (18), were found for the first time in the extracts. Our results showed that the biological activities of this plant might be linked to their phenolic compounds and that the polar extracts could be considered as new natural supplements to be used in food and pharmaceuticals.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8272662PMC
http://dx.doi.org/10.1155/2021/6675436DOI Listing

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