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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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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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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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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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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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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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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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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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Effects of Sodium Nitroprusside on Lipopolysaccharide-Induced Inflammation and Disruption of Blood-Brain Barrier

Cells (Basel, Switzerland), 2024-05, Vol.13 (10), p.843

2024

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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 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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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

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

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

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

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

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

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?

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

Effects of Sodium Nitroprusside on Lipopolysaccharide-Induced Inflammation and Disruption of Blood-Brain Barrier

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

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

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