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Phytochemical Analysis and Antiproliferative Activity of Ulex gallii Planch. (Fabaceae), a Medicinal Plant from Galicia (Spain)

Molecules (Basel, Switzerland), 2023-01, Vol.28 (1), p.351

2023

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Coumarin-Resveratrol-Inspired Hybrids as Monoamine Oxidase B Inhibitors: 3-Phenylcoumarin versus trans -6-Styrylcoumarin

Molecules (Basel, Switzerland), 2022-01, Vol.27 (3), p.928

2022

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Curcumin–Coumarin Hybrid Analogues as Multitarget Agents in Neurodegenerative Disorders

Molecules (Basel, Switzerland), 2021-07, Vol.26 (15), p.4550

2021

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A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors

Bioorganic & medicinal chemistry letters, 2009-06, Vol.19 (12), p.3268-3270

2009

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Combined 3D-QSAR and docking analysis for the design and synthesis of chalcones as potent and selective monoamine oxidase B inhibitors

Bioorganic chemistry, 2021-03, Vol.108, p.104689-104689, Article 104689

2021

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3-Arylcoumarins as highly potent and selective monoamine oxidase B inhibitors: Which chemical features matter?

Bioorganic chemistry, 2020-08, Vol.101, p.103964, Article 103964

2020

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Synthesis and in vitro study of nitro- and methoxy-2-phenylbenzofurans as human monoamine oxidase inhibitors

Bioorganic chemistry, 2021-02, Vol.107, p.104616-104616, Article 104616

2021

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New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors

Bioorganic & medicinal chemistry letters, 2010-09, Vol.20 (17), p.5157-5160

2010

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Antitumor activity of copper(II) complexes with Schiff bases derived from N'-tosylbenzene-1,2-diamine

Journal of inorganic biochemistry, 2022-11, Vol.236, p.111975-111975, Article 111975

2022

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Regioselective Synthesis of 1-Alkyl- or 1-Aryl-1H-indazoles via Copper-Catalyzed Cyclizations of 2-Haloarylcarbonylic Compounds

Organic letters, 2007-02, Vol.9 (3), p.525-528

2007

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Discovery and optimization of 3-thiophenylcoumarins as novel agents against Parkinson’s disease: Synthesis, in vitro and in vivo studies

Bioorganic chemistry, 2020-08, Vol.101, p.103986, Article 103986

2020

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Synthesis, biological evaluation and molecular modeling studies of phthalazin-1(2H)-one derivatives as novel cholinesterase inhibitors

RSC advances, 2016-01, Vol.6 (52), p.46170-46185

2016

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Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-halo-3-phenylcoumarins

Molecules (Basel, Switzerland), 2010-01, Vol.15 (1), p.270-279

2010

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Hydroxycoumarins as selective MAO-B inhibitors

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (1), p.258-261

2012

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Design, Synthesis and Docking Calculations of Prenylated Chalcones as Selective Monoamine Oxidase B Inhibitors with Antioxidant Activity

ChemistrySelect (Weinheim), 2019-07, Vol.4 (26), p.7698-7703

2019

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Synthesis of 3′- O-phosphonomethyl nucleosides with an adenine base moiety

Tetrahedron, 2007-03, Vol.63 (12), p.2634-2646

2007

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Pyrazolo[3,4,5- de]phthalazine. Syntheses of a practically unknown heterocyclic system

Tetrahedron, 2009-02, Vol.65 (8), p.1574-1580

2009

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Synthesis of Carbocyclic Pyrimidine Nucleosides Using the Mitsunobu Reaction: O 2 ‐ vs. N 1 ‐Alkylation

Helvetica chimica acta, 2010-02, Vol.93 (2), p.309-313

2010

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NEW BUTYROLACTONE FROM A MARINE-DERIVED FUNGUS ASPERGILLUS SP

Journal of the Chilean Chemical Society, 2011, Vol.56 (1), p.625-627

2011

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QSAR for anti-RNA-virus activity, synthesis, and assay of anti-RSV carbonucleosides given a unified representation of spectral moments, quadratic, and topologic indices

Bioorganic & medicinal chemistry letters, 2005-03, Vol.15 (6), p.1651-1657

2005

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Regioselective synthesis of O 2- and O 6-cyclopyrimidine nucleoside analogues

Tetrahedron, 2006-10, Vol.62 (42), p.9949-9952

2006

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Stochastic entropy QSAR for the in silico discovery of anticancer compounds: Prediction, synthesis, and in vitro assay of new purine carbanucleosides

Bioorganic & medicinal chemistry, 2006-02, Vol.14 (4), p.1095-1107

2006

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Synthesis of Regioisomeric Functionalized Benzodifurans and Angelicins

Helvetica chimica acta, 2009-07, Vol.92 (7), p.1309-1314

2009

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1,2-Disubstituted cyclohexane nucleosides: comparative study for the synthesis of cis and trans adenosine analogues

Tetrahedron, 2005-01, Vol.61 (2), p.473-478

2005

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Synthesis of 1,2-Disubstituted Carbocyclic Nucleoside Analogues of Cytidine

Helvetica chimica acta, 2006-05, Vol.89 (5), p.954-961

2006

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Phytochemical Analysis and Antiproliferative Activity of Ulex gallii Planch. (Fabaceae), a Medicinal Plant from Galicia (Spain)

Coumarin-Resveratrol-Inspired Hybrids as Monoamine Oxidase B Inhibitors: 3-Phenylcoumarin versus trans -6-Styrylcoumarin

Curcumin–Coumarin Hybrid Analogues as Multitarget Agents in Neurodegenerative Disorders

A new series of 3-phenylcoumarins as potent and selective MAO-B inhibitors

Combined 3D-QSAR and docking analysis for the design and synthesis of chalcones as potent and selective monoamine oxidase B inhibitors

3-Arylcoumarins as highly potent and selective monoamine oxidase B inhibitors: Which chemical features matter?

Synthesis and in vitro study of nitro- and methoxy-2-phenylbenzofurans as human monoamine oxidase inhibitors

New halogenated 3-phenylcoumarins as potent and selective MAO-B inhibitors

Antitumor activity of copper(II) complexes with Schiff bases derived from N'-tosylbenzene-1,2-diamine

Regioselective Synthesis of 1-Alkyl- or 1-Aryl-1H-indazoles via Copper-Catalyzed Cyclizations of 2-Haloarylcarbonylic Compounds

Discovery and optimization of 3-thiophenylcoumarins as novel agents against Parkinson’s disease: Synthesis, in vitro and in vivo studies

Synthesis, biological evaluation and molecular modeling studies of phthalazin-1(2H)-one derivatives as novel cholinesterase inhibitors

Synthesis and vasorelaxant and platelet antiaggregatory activities of a new series of 6-halo-3-phenylcoumarins

Hydroxycoumarins as selective MAO-B inhibitors

Design, Synthesis and Docking Calculations of Prenylated Chalcones as Selective Monoamine Oxidase B Inhibitors with Antioxidant Activity

Synthesis of 3′- O-phosphonomethyl nucleosides with an adenine base moiety

Pyrazolo[3,4,5- de]phthalazine. Syntheses of a practically unknown heterocyclic system

Synthesis of Carbocyclic Pyrimidine Nucleosides Using the Mitsunobu Reaction: O 2 ‐ vs. N 1 ‐Alkylation

NEW BUTYROLACTONE FROM A MARINE-DERIVED FUNGUS ASPERGILLUS SP

QSAR for anti-RNA-virus activity, synthesis, and assay of anti-RSV carbonucleosides given a unified representation of spectral moments, quadratic, and topologic indices

Regioselective synthesis of O 2- and O 6-cyclopyrimidine nucleoside analogues

Stochastic entropy QSAR for the in silico discovery of anticancer compounds: Prediction, synthesis, and in vitro assay of new purine carbanucleosides

Synthesis of Regioisomeric Functionalized Benzodifurans and Angelicins

1,2-Disubstituted cyclohexane nucleosides: comparative study for the synthesis of cis and trans adenosine analogues

Synthesis of 1,2-Disubstituted Carbocyclic Nucleoside Analogues of Cytidine

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