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Anti-tyrosinase, anti-cholinesterase and cytotoxic activities of extracts and phytochemicals from the Tunisian Citharexylum spinosum L.: Molecular docking and SAR analysis.
- Source :
-
Bioorganic chemistry [Bioorg Chem] 2020 Sep; Vol. 102, pp. 104093. Date of Electronic Publication: 2020 Jul 14. - Publication Year :
- 2020
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Abstract
- Previously phytochemical investigations carried out on the flowers and trunk bark extracts of Citharexylum spinosum L. tree, allowed the isolation of twenty molecules belonging to several families of natural substances [triterpene acids, iridoid glycosides, phenylethanoid glycosides, 8,3'-neolignan glycosides, together with other phenolic compounds]. In the present work, a biological evaluation (anti-tyrosinase, anticholinesterase and cytotoxic activities) was performed on the prepared extracts and the isolated secondary metabolites. The results showed that the EtOAc extract of the trunk bark displayed the highest anti-tyrosinase effect with a percent inhibition of 55.0 ± 1.8% at a concentration of 100 µg/mL. The highest anticholinesterase activity was presented by the same extract with an IC <subscript>50</subscript> value of 99.97 ± 3.01 µg/mL. The EtOAc extract of flowers and that of the trunk bark displayed the best cytotoxic property with IC <subscript>50</subscript> values of 96.00 ± 2.85 and 88.75 ± 2.00 µg/mL, respectively, against the human cervical cancer cell line (HeLa), and IC <subscript>50</subscript> values of 188.23 ± 3.88 and 197.00 ± 4.25 µg/mL, respectively, against the human lung cancer (A549) cell lines. Biological investigation of the pure compounds showed that the two 8,3'-neolignan glycosides, plucheosides D <subscript>1</subscript> -D <subscript>2</subscript> , generate the highest anti-tyrosinase potency with a percent inhibition of 61.4 ± 2.0 and 79.5 ± 2.3%, respectively, at a concentration of 100 µM. The iridoid glycosides exhibited a significant anticholinesterase activity with IC <subscript>50</subscript> values ranging from 17.19 ± 1.02 to 52.24 ± 2.50 µM. Triterpene pentacyclic acids and iridoid glycosides exerted encouraging cytotoxic effects against HeLa with IC <subscript>50</subscript> values ranging from 9.00 ± 1.10 to 25.00 ± 1.00 µM. The study of the structure-activity relationship (SAR) has been sufficiently and widely discussed. The natural compounds that exhibited the significant bioactivities were docked.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2020. Published by Elsevier Inc.)
- Subjects :
- Animals
Antineoplastic Agents, Phytogenic chemistry
Antineoplastic Agents, Phytogenic isolation & purification
Cell Line
Cell Proliferation drug effects
Cholinesterases metabolism
Dose-Response Relationship, Drug
Drug Screening Assays, Antitumor
Enzyme Inhibitors chemistry
Enzyme Inhibitors isolation & purification
Humans
Mice
Molecular Structure
Monophenol Monooxygenase antagonists & inhibitors
Monophenol Monooxygenase metabolism
Phytochemicals chemistry
Phytochemicals isolation & purification
Plant Extracts chemistry
Plant Extracts isolation & purification
Structure-Activity Relationship
Antineoplastic Agents, Phytogenic pharmacology
Enzyme Inhibitors pharmacology
Molecular Docking Simulation
Phytochemicals pharmacology
Plant Extracts pharmacology
Verbenaceae chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2120
- Volume :
- 102
- Database :
- MEDLINE
- Journal :
- Bioorganic chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 32717693
- Full Text :
- https://doi.org/10.1016/j.bioorg.2020.104093