Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/33260
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dc.contributor.authorTusevski, Oliveren_US
dc.contributor.authorTodorovska, Marijaen_US
dc.contributor.authorPetreska Stanoeva, Jasminaen_US
dc.contributor.authorGadzovska Simic, Sonjaen_US
dc.date.accessioned2025-04-16T08:52:30Z-
dc.date.available2025-04-16T08:52:30Z-
dc.date.issued2024-08-17-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/33260-
dc.description.abstract<jats:p>Hypericum perforatum transformed shoot lines (TSL) regenerated from corresponding hairy roots and non-transformed shoots (NTS) were comparatively evaluated for their phenolic compound contents and in vitro inhibitory capacity against target enzymes (monoamine oxidase-A, cholinesterases, tyrosinase, α-amylase, α-glucosidase, lipase, and cholesterol esterase). Molecular docking was conducted to assess the contribution of dominant phenolic compounds to the enzyme-inhibitory properties of TSL samples. The TSL extracts represent a rich source of chlorogenic acid, epicatechin and procyanidins, quercetin aglycone and glycosides, anthocyanins, naphthodianthrones, acyl-phloroglucinols, and xanthones. Concerning in vitro bioactivity assays, TSL displayed significantly higher acetylcholinesterase, tyrosinase, α-amylase, pancreatic lipase, and cholesterol esterase inhibitory properties compared to NTS, implying their neuroprotective, antidiabetic, and antiobesity potential. The docking data revealed that pseudohypericin, hyperforin, cadensin G, epicatechin, and chlorogenic acid are superior inhibitors of selected enzymes, exhibiting the lowest binding energy of ligand–receptor complexes. Present data indicate that H. perforatum transformed shoots might be recognized as an excellent biotechnological system for producing phenolic compounds with multiple health benefits.</jats:p>en_US
dc.publisherMDPI AGen_US
dc.relation.ispartofMoleculesen_US
dc.titlePhytochemical Analysis, Biological Activities, and Docking of Phenolics from Shoot Cultures of Hypericum perforatum L. Transformed by Agrobacterium rhizogenesen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/molecules29163893-
dc.identifier.urlhttps://www.mdpi.com/1420-3049/29/16/3893/pdf-
dc.identifier.volume29-
dc.identifier.issue16-
dc.identifier.fpage3893-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Philosophy-
Appears in Collections:Faculty of Natural Sciences and Mathematics, Institute of Biology: Journal Articles
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