EUGENIO
URIARTE VILLARES
Catedrático de universidade
University of Cagliari
Cagliari, ItaliaPublicacións en colaboración con investigadores/as de University of Cagliari (51)
2023
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2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol. 38, Núm. 1
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Design of 3-Phenylcoumarins and 3-Thienylcoumarins as Potent Xanthine Oxidase Inhibitors: Synthesis, Biological Evaluation, and Docking Studies
ChemMedChem, Vol. 18, Núm. 21
2022
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Coumarin-Resveratrol-Inspired Hybrids as Monoamine Oxidase B Inhibitors: 3-Phenylcoumarin versus trans-6-Styrylcoumarin
Molecules, Vol. 27, Núm. 3
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Hydroxy-3-Phenylcoumarins as Multitarget Compounds for Skin Aging Diseases: Synthesis, Molecular Docking and Tyrosinase, Elastase, Collagenase and Hyaluronidase Inhibition, and Sun Protection Factor
Molecules, Vol. 27, Núm. 20
2020
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Looking for new xanthine oxidase inhibitors: 3-Phenylcoumarins versus 2-phenylbenzofurans
International Journal of Biological Macromolecules, Vol. 162, pp. 774-780
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Structure-Based Optimization of Coumarin hA3 Adenosine Receptor Antagonists
Journal of Medicinal Chemistry, Vol. 63, Núm. 5, pp. 2577-2587
2019
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Antibacterial Activity and Molecular Docking Studies of a Selected Series of Hydroxy-3-arylcoumarins
Molecules (Basel, Switzerland), Vol. 24, Núm. 15
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Discovery of new phthalazinones as vasodilator agents and novel pharmacological tools to study calcium channels
Future Medicinal Chemistry, Vol. 11, Núm. 3, pp. 179-191
2018
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Coumarin derivatives as promising xanthine oxidase inhibitors
International Journal of Biological Macromolecules, Vol. 120, pp. 1286-1293
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Evaluation of trypanocidal and antioxidant activities of a selected series of 3-amidocoumarins
Medicinal Chemistry, Vol. 14, Núm. 6, pp. 573-584
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Targeting α -(1,4)-glucosidase in diabetes mellitus type 2: The role of new synthetic coumarins as potent inhibitors
Current Topics in Medicinal Chemistry, Vol. 18, Núm. 27, pp. 2327-2337
2017
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New insights into highly potent tyrosinase inhibitors based on 3-heteroarylcoumarins: Anti-melanogenesis and antioxidant activities, and computational molecular modeling studies
Bioorganic and Medicinal Chemistry, Vol. 25, Núm. 5, pp. 1687-1695
2016
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Progress in the development of small molecules as new human A3 adenosine receptor ligands based on the 3-thiophenylcoumarin core
MedChemComm, Vol. 7, Núm. 5, pp. 845-852
2015
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Design and discovery of tyrosinase inhibitors based on a coumarin scaffold
RSC Advances, Vol. 5, Núm. 114, pp. 94227-94235
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Interest of 3-arylcoumarins as xanthine oxidase inhibitors
19TH INTERNATIONAL ELECTRONIC CONFERENCE ON SYNTHETIC ORGANIC CHEMISTRY
2014
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Monoamine oxidase (MAO) inhibitory activity: 3-phenylcoumarins versus 4-hydroxy-3-phenylcoumarins
ChemMedChem, Vol. 9, Núm. 8, pp. 1672-1676
2013
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MAO Inhibitory Activity of 2-Arylbenzofurans versus 3-Arylcoumarins: Synthesis, invitro Study, and Docking Calculations
ChemMedChem, Vol. 8, Núm. 6, pp. 956-966
2012
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8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies
ChemMedChem, Vol. 7, Núm. 3, pp. 464-470
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Antitrypanosomal and antioxidant properties of 4-hydroxycoumarins derivatives
Bioorganic and Medicinal Chemistry Letters, Vol. 22, Núm. 17, pp. 5569-5573
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Erratum: Synthesis and cytotoxic activity of non-naturally substituted 4-oxycoumarin derivatives (Bioorganic and Medicinal Chemistry Letters (2012) 22 (5791-5794))
Bioorganic and Medicinal Chemistry Letters