Evidence map›Paper›PMID 42860876›Full record

ArticleChemistry & biodiversity2026

Green Extraction of Phenolic Compounds From Pistacia lentiscus Leaves Coupled With LC-MS Characterization and Structure-Based Enzyme Inhibition Analysis.

Sidali Zaidi, Naima Saidene, Radia Kadi, Nadjet Benaida-Debbache

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Article in Chemistry & biodiversity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Sidali ZaidiCentre de Recherche en Technologies Agro-Alimentaires, Campus Universitaire, Bejaia, Algeria.ORCID https://orcid.org/0000-0001-7368-9054
Naima SaideneFaculté Des Sciences de La Nature Et de La Vie, Laboratoire de Biochimie Appliquée, Université de Bejaia, Bejaia, Algeria.
Radia KadiFaculté Des Sciences de La Nature Et de La Vie, Laboratoire de Biomathématique, Biophysique, Biochimie Et Scientométrie (3BS), Université de Bejaia, Bejaia, Algeria.
Nadjet Benaida-DebbacheFaculté Des Sciences de La Nature Et de La Vie, Laboratoire de Biochimie Appliquée, Université de Bejaia, Bejaia, Algeria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acetylcholinesterase (AChE) and urease are critical enzymes involved in various pathological conditions associated with cellular and tissue damage. Natural products are increasingly explored as safer alternatives to synthetic inhibitors. This study evaluates the phytochemical composition and enzyme inhibitory potential of Pistacia lentiscus leaves using a green extraction approach. Bioactive compounds were extracted via lactic acid-assisted ultrasound, and the crude extract was characterized for total phenolics, flavonoids, LC-MS profile, and in vitro inhibition of acetylcholinesterase and urease. Molecular docking was performed to investigate ligand-enzyme interactions. The extract contained 142.13 ± 0.06 mg GAE/g DW of polyphenols and 16.17 ± 0.02 mg QE/g DW of flavonoids. LC-MS analysis identified phenolic acids, phenolic glycosides, coumarins, and multiple flavonoid subclasses, including flavonols, flavanols, flavanones, flavones, and flavonolignans. The extract exhibited significant inhibition of both enzymes. Docking studies revealed key interactions, such as hydrogen bonds, π-alkyl, and π-sigma, within the active sites, with hesperidin and verbascoside showing the strongest binding affinities (acetylcholinesterase: -10.1 and -10.2 kcal/mol; urease: -9.6 and -9.2 kcal/mol, respectively). These results demonstrate that ultrasound-assisted lactic acid extraction efficiently isolates phenolic compounds from P. lentiscus, and the identified metabolites may serve as promising templates for the development of potent enzyme inhibitors.

Indexed as

Cholinesterase InhibitorsEnzyme InhibitorsPhenolsPistaciaPlant ExtractsUreaseAcetylcholinesteraseChromatography, LiquidGreen Chemistry TechnologyMass SpectrometryMolecular Docking SimulationMolecular StructurePlant LeavesStructure-Activity RelationshipAcetylcholinesteraseCholinesterase InhibitorsEnzyme InhibitorsPhenolsPlant ExtractsUreaseenzymatic activitieslactic acidmolecular dockingP. lentiscusultrasound‐assisted extraction

Identifiers

PMID42860876
PMCPMC13655636

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