Departamento de Farmacoloxía, Farmacia e Tecnoloxía Farmacéutica
Departamento
University of Cagliari
Cagliari, ItaliaPublicacións en colaboración con investigadores/as de University of Cagliari (24)
2023
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Villoglandular Pattern in HPV-associated Endocervical Adenocarcinoma is Associated with Excellent Prognosis: A Reappraisal of 31 Cases Using IECC and Silva Pattern Classification
International Journal of Gynecological Pathology, Vol. 42, Núm. 3, pp. 270-277
2022
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Clear Cell Carcinoma (CCC) of the Cervix Is a Human Papillomavirus (HPV)-independent Tumor Associated With Poor Outcome A Comprehensive Analysis of 58 Cases
American Journal of Surgical Pathology, Vol. 46, Núm. 6, pp. 765-773
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Coumarin-Resveratrol-Inspired Hybrids as Monoamine Oxidase B Inhibitors: 3-Phenylcoumarin versus trans-6-Styrylcoumarin
Molecules, Vol. 27, Núm. 3
2021
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Gamma-decanolactone: Preliminary evaluation as potential antiparkinsonian drug
European Journal of Pharmacology, Vol. 906
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Synthesis and in vitro study of nitro- and methoxy-2-phenylbenzofurans as human monoamine oxidase inhibitors
Bioorganic Chemistry, Vol. 107
2019
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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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Novel 2-pheynlbenzofuran derivatives as selective butyrylcholinesterase inhibitors for Alzheimer's disease
Scientific Reports, Vol. 8, Núm. 1
2017
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MAO inhibitory activity of bromo-2-phenylbenzofurans: Synthesis,: in vitro study, and docking calculations
MedChemComm, Vol. 8, Núm. 9, pp. 1788-1796
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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A novel series of 3,4-disubstituted dihydropyrazoles: Synthesis and evaluation for MAO enzyme inhibition
Journal of Heterocyclic Chemistry, Vol. 50, Núm. SUPPL.1
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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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Herbal natural products as a source of monoamine oxidase inhibitors: A review
Current Topics in Medicinal Chemistry, Vol. 12, Núm. 20, pp. 2131-2144
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Hydroxycoumarins as selective MAO-B inhibitors
Bioorganic and Medicinal Chemistry Letters, Vol. 22, Núm. 1, pp. 258-261
2011
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Synthesis, human monoamine oxidase inhibitory activity and molecular docking studies of 3-heteroarylcoumarin derivatives
European Journal of Medicinal Chemistry, Vol. 46, Núm. 4, pp. 1147-1152
2010
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Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-Halo-3-phenylcoumarins
Molecules, Vol. 15, Núm. 1, pp. 270-279
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Synthesis of carbocyclic pyrimidine nucleosides using the Mitsunobu reaction: O2- vs. N1-alkylation
Helvetica Chimica Acta, Vol. 93, Núm. 2, pp. 309-313
2009
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Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors
Bioorganic and Medicinal Chemistry Letters, Vol. 19, Núm. 17, pp. 5053-5055
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Synthesis of regioisomeric functionalized benzodifurans and angelicins
Helvetica Chimica Acta, Vol. 92, Núm. 7, pp. 1309-1314
2008
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Synthesis and complete assignment of the 1H and 13C NMR signals of some oxopyrancoumarin and oxofuropyrancoumarin derivatives
Magnetic Resonance in Chemistry, Vol. 46, Núm. 7, pp. 701-705