Enzo Cadoni

Publications84
h-index12
Citations647
Highly Influential Citations7
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Supercritical CO2 extraction of lycopene and β-carotene from ripe tomatoes
Abstract This work describes the influence of some operative parameters of supercritical carbon dioxide extraction employed for the isolation of lycopene and β-carotene from the pulp and skins of… Expand
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Hydroxycoumarins as selective MAO-B inhibitors.
A series of 3-aryl-4-hydroxycoumarin derivatives was synthesized with the aim to find out the structural features for the MAO inhibitory activity and selectivity. Methoxy and/or chloro substituents… Expand
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MAO Inhibitory Activity of 2‐Arylbenzofurans versus 3‐Arylcoumarins: Synthesis, in vitro Study, and Docking Calculations
Monoamine oxidase (MAO) is an important drug target for the treatment of neurological disorders. Several 3‐arylcoumarin derivatives were previously described as interesting selective MAO‐B… Expand
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Liquid-phase thiophene adsorption on MCM-22 zeolite and activated carbon
Abstract The liquid-phase adsorption of thiophene from thiophene/ iso -octane and toluene-rich thiophene/toluene/ iso -octane solutions has been investigated in batch conditions at room temperature… Expand
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Structural Diversity in a New Series of Halogenated Quinolyl Salicylaldimides-Based FeIII Complexes Showing Solid-State Halogen-Bonding/Halogen···Halogen Interactions
A new series of tridentate N-8-quinolyl-salicylaldimine ligands, Hqsal-5,7-X2 [X = Cl(1), Br(2), I(3)], halo-substituted at the 5,7 position of the aminoquinoline moiety and their corresponding… Expand
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8‐Substituted 3‐Arylcoumarins as Potent and Selective MAO‐B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies
Neurodegenerative disorders are becoming more prevalent given the increase in the aging population. This has inspired active research in the development of new drugs that could mark an important… Expand
  • 41
Monoamine oxidase inhibitors: ten years of docking studies.
The number of papers dealing with the structure-based drug design is continuously growing, which demonstrates the importance of such tools in medicinal chemistry. In the current paper, the published… Expand
  • 19
Novel coumarins and related copper complexes with biological activity: DNA binding, molecular docking and in vitro antiproliferative activity.
Coumarins show biological activity and are widely exploited for their therapeutic effects. Although a great number of coumarins substituted by heterocyclic moieties have been prepared, few studies… Expand
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Competitive reactions among glutathione, cisplatin and copper-phenanthroline complexes.
A large number of cancers are treated with cisplatin (CDDP). However, its use is limited by drug resistance, which is often related to intracellular levels of thiol-containing molecules such as… Expand
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A re-examination of the methylenation reaction
A re-examination of the methylenation reaction of 1-hydroxy-2-mercapto-, 1,2-dihydroxy- and 1,2-dimercapto-substituted benzenes by bromochloromethane with cesium carbonate shows that these substrates… Expand
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