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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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Heterocycle-containing tranylcypromine derivatives endowed with high anti-LSD1 activity

Journal of enzyme inhibition and medicinal chemistry, 2022-12, Vol.37 (1), p.973-985

2022

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New flavonoid - N,N-dibenzyl(N-methyl)amine hybrids: Multi-target-directed agents for Alzheimer´s disease endowed with neurogenic properties

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.712-727

2019

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Coumarin analogue 3-methyl-7H-furo[3,2-g] chromen-7-one as a possible antiparkinsonian agent

Biomedica : revista del Instituto Nacional de Salud, 2019-09, Vol.39 (3), p.491-501

2019

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Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors

Journal of medicinal chemistry, 2011-10, Vol.54 (20), p.7127-7137

2011

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Nanomolar resveratrol reduces early alterations of pancreatitis and pancreatic cancer in pancreatic acinar cells

Phytomedicine Plus : International journal of phytotherapy and phytopharmacology, 2022-08, Vol.2 (3), p.100301, Article 100301

2022

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Novel 2-pheynlbenzofuran derivatives as selective butyrylcholinesterase inhibitors for Alzheimer's disease

Scientific reports, 2018-03, Vol.8 (1), p.4424-12, Article 4424

2018

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Dual inhibitors of monoamine oxidase and cholinesterase for the treatment of Alzheimer disease

Current topics in medicinal chemistry, 2013-08, Vol.13 (14), p.1692

2013

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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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Alignment-Free Prediction of a Drug−Target Complex Network Based on Parameters of Drug Connectivity and Protein Sequence of Receptors

Molecular pharmaceutics, 2009-06, Vol.6 (3), p.825-835

2009

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Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (17), p.5053-5055

2009

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cAMP Compartmentalization in Cerebrovascular Endothelial Cells: New Therapeutic Opportunities in Alzheimer’s Disease

Cells (Basel, Switzerland), 2021-07, Vol.10 (8), p.1951

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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Quantitative Structure−Activity Relationship and Complex Network Approach to Monoamine Oxidase A and B Inhibitors

Journal of medicinal chemistry, 2008-11, Vol.51 (21), p.6740-6751

2008

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Herbal natural products as a source of monoamine oxidase inhibitors: a review

Current topics in medicinal chemistry, 2012-10, Vol.12 (20), p.2131

2012

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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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Focusing on new monoamine oxidase inhibitors: differently substituted coumarins as an interesting scaffold

Current topics in medicinal chemistry, 2012-10, Vol.12 (20), p.2210

2012

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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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Coumarin‐Rasagiline Hybrids as Potent and Selective hMAO‐B Inhibitors, Antioxidants, and Neuroprotective Agents

ChemMedChem, 2020-03, Vol.15 (6), p.532-538

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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Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

European journal of medicinal chemistry, 2017-10, Vol.139, p.1-11

2017

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Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (2), p.707-709

2011

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7‐Amidocoumarins as Multitarget Agents against Neurodegenerative Diseases: Substitution Pattern Modulation

ChemMedChem, 2021-01, Vol.16 (1), p.179-186

2021

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Chromone, a Privileged Scaffold for the Development of Monoamine Oxidase Inhibitors

Journal of medicinal chemistry, 2011-07, Vol.54 (14), p.5165-5173

2011

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

Heterocycle-containing tranylcypromine derivatives endowed with high anti-LSD1 activity

New flavonoid - N,N-dibenzyl(N-methyl)amine hybrids: Multi-target-directed agents for Alzheimer´s disease endowed with neurogenic properties

Coumarin analogue 3-methyl-7H-furo[3,2-g] chromen-7-one as a possible antiparkinsonian agent

Synthesis and Study of a Series of 3-Arylcoumarins as Potent and Selective Monoamine Oxidase B Inhibitors

Nanomolar resveratrol reduces early alterations of pancreatitis and pancreatic cancer in pancreatic acinar cells

Novel 2-pheynlbenzofuran derivatives as selective butyrylcholinesterase inhibitors for Alzheimer's disease

Dual inhibitors of monoamine oxidase and cholinesterase for the treatment of Alzheimer disease

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

Alignment-Free Prediction of a Drug−Target Complex Network Based on Parameters of Drug Connectivity and Protein Sequence of Receptors

Synthesis and evaluation of 6-methyl-3-phenylcoumarins as potent and selective MAO-B inhibitors

cAMP Compartmentalization in Cerebrovascular Endothelial Cells: New Therapeutic Opportunities in Alzheimer’s Disease

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

Quantitative Structure−Activity Relationship and Complex Network Approach to Monoamine Oxidase A and B Inhibitors

Herbal natural products as a source of monoamine oxidase inhibitors: a review

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

Focusing on new monoamine oxidase inhibitors: differently substituted coumarins as an interesting scaffold

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

Coumarin‐Rasagiline Hybrids as Potent and Selective hMAO‐B Inhibitors, Antioxidants, and Neuroprotective Agents

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

Synthesis and structure-activity relationship study of novel 3-heteroarylcoumarins based on pyridazine scaffold as selective MAO-B inhibitors

Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors

7‐Amidocoumarins as Multitarget Agents against Neurodegenerative Diseases: Substitution Pattern Modulation

Chromone, a Privileged Scaffold for the Development of Monoamine Oxidase Inhibitors

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