NATURAL PRODUCT COMMUNICATIONS, cilt.19, sa.8, ss.1-9, 2024 (SCI-Expanded)
Abstract
Objective: In our study, we researched the chemical composition of Linaria corifolia Desf. We also tested in vitro antioxidant, and
anticholinesterase activities of different extracts, and compounds from L. corifolia. Methods: We isolated from ethyl acetate and
n-butanol extracts of L. corifolia aerial parts. We used various spectroscopic methods. We also compared the results with data in
the literature. This allowed us to determine the structure of the compounds. We used different spectroscopic methods and compar-
isons with literature data to determine the structure of the compounds. We evaluated the antioxidant activities of 20% aqueous meth-
anol, ethyl acetate, and n-butanol extracts using DPPH, ABTS Radical Scavenging Effect, and CUPRAC Assay, and also examined
total phenol and flavonoid contents. We used Ellman’s method to find the cholinesterase inhibitor activities of the extracts, and
isolated compounds. Results: We isolated 6 compounds in ethyl acetate and n-butanol extracts. These compounds have terpenoid
(iridoid glycosides), and phenolics (flavonoid, and phenylpropanoid structures). We isolated linariin and acteoside (verbascoside)
from ethyl acetate. We isolated antirrhinoside, 6-ß-Hydroxyantirrhide, catalpol, and aucubin from n-butanol extract. The ethyl
acetate extract was most active in all antioxidant methods due to its high phenolic content. In contrast to phenolic content, n-
butanol extract had more flavonoids. The ethyl acetate extract had higher acetylcholinesterase inhibitory activity at 200 and 400
μg/ml. Linariin had the highest acetylcholinesterase inhibitory effect among the pure compounds. The extracts and pure compounds
inhibited butyrylcholinesterase less than acetylcholinesterase. Conclusion: The isolated compounds are new compounds for the L.
corifolia plant. The plant’s cholinesterase inhibitor activity was investigated for the first time. We found low anti-acetylcholinesterase
and butyrylcholinesterase activities.