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1,3,4-Oxadiazol-2-ylbenzenesulfonamides as privileged structures for the inhibition of monoamine oxidase B

Bioorganic & medicinal chemistry letters, 2019-11, Vol.29 (21), p.126677-126677, Article 126677

2019

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2-acetylphenol analogs as potent reversible monoamine oxidase inhibitors

Drug design, development and therapy, 2015-01, Vol.9 (default), p.3635-3644

2015

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2-Aminopyrimidines as dual adenosine A1/A2A antagonists

European journal of medicinal chemistry, 2015-11, Vol.104, p.177-188

2015

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2-Benzylidene-1-indanone derivatives as inhibitors of monoamine oxidase

Bioorganic & medicinal chemistry letters, 2016-10, Vol.26 (19), p.4599-4605

2016

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2-Heteroarylidene-1-indanone derivatives as inhibitors of monoamine oxidase

Bioorganic chemistry, 2016-12, Vol.69, p.20-28

2016

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3--1,2,4-oxadiazole

MolBank, 2023-01, Vol.2023 (1)

2023

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3-(3,4-Dichlorophenyl)-5-(1H-indol-5-yl)-1,2,4-oxadiazole

MolBank, 2023-03, Vol.2023 (1), p.M1552

2023

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3-Coumaranone derivatives as inhibitors of monoamine oxidase

Drug design, development and therapy, 2015-01, Vol.9 (default), p.5479-5489

2015

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4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.597-612

2019

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8-(3-Chlorostyryl)caffeine May Attenuate MPTP Neurotoxicity through Dual Actions of Monoamine Oxidase Inhibition and A2A Receptor Antagonism

The Journal of biological chemistry, 2002-09, Vol.277 (39), p.36040-36044

2002

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8-Aryl- and alkyloxycaffeine analogues as inhibitors of monoamine oxidase

European journal of medicinal chemistry, 2011-08, Vol.46 (8), p.3474-3485

2011

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The adenosine A(2A) antagonistic properties of selected C8-substituted xanthines

Bioorganic chemistry, 2013-08, Vol.49, p.49-58

2013

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The adenosine A2A antagonistic properties of selected C8-substituted xanthines

Bioorganic chemistry, 2013-08, Vol.49, p.49-58

2013

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The adenosine receptor affinities and monoamine oxidase B inhibitory properties of sulfanylphthalimide analogues

Bioorganic chemistry, 2015-04, Vol.59, p.117-123

2015

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α-Tetralone derivatives as inhibitors of monoamine oxidase

Bioorganic & medicinal chemistry letters, 2014-06, Vol.24 (12), p.2758-2763

2014

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Azure B, a metabolite of methylene blue, is a high-potency, reversible inhibitor of monoamine oxidase

Toxicology and applied pharmacology, 2012-02, Vol.258 (3), p.403-409

2012

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Azure B and a synthetic structural analogue of methylene blue, ethylthioninium chloride, present with antidepressant-like properties

Life sciences (1973), 2014-11, Vol.117 (2), p.56-66

2014

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Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.1511-1525

2019

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Benzyloxynitrostyrene analogues – A novel class of selective and highly potent inhibitors of monoamine oxidase B

European journal of medicinal chemistry, 2017-01, Vol.125, p.1193-1199

2017

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Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor

Molecules (Basel, Switzerland), 2021-07, Vol.26 (15), p.4599

2021

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Caffeine as a lead compound for the design of therapeutic agents for the treatment of Parkinson's disease

Current medicinal chemistry, 2015-01, Vol.22 (8), p.975

2015

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Carbamate substituted 2-amino-4,6-diphenylpyrimidines as adenosine receptor antagonists

Bioorganic & medicinal chemistry letters, 2016-02, Vol.26 (3), p.734-738

2016

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Chapter 5 - Multifunctional Enzyme Inhibition for Neuroprotection - A Focus on MAO, NOS, and AChE Inhibitors

Drug Design and Discovery in Alzheimer’s Disease, 2015, p.291-365

2015

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Coumarin-Based Dual Inhibitors of Human Carbonic Anhydrases and Monoamine Oxidases Featuring Amino Acyl and ( Pseudo )-Dipeptidyl Appendages: In Vitro and Computational Studies

Molecules (Basel, Switzerland), 2022-11, Vol.27 (22), p.7884

2022

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Coumarin derivatives as inhibitors of d-amino acid oxidase and monoamine oxidase

Bioorganic chemistry, 2022-06, Vol.123, p.105791-105791, Article 105791

2022

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1,3,4-Oxadiazol-2-ylbenzenesulfonamides as privileged structures for the inhibition of monoamine oxidase B

2-acetylphenol analogs as potent reversible monoamine oxidase inhibitors

2-Aminopyrimidines as dual adenosine A1/A2A antagonists

2-Benzylidene-1-indanone derivatives as inhibitors of monoamine oxidase

2-Heteroarylidene-1-indanone derivatives as inhibitors of monoamine oxidase

3--1,2,4-oxadiazole

3-(3,4-Dichlorophenyl)-5-(1H-indol-5-yl)-1,2,4-oxadiazole

3-Coumaranone derivatives as inhibitors of monoamine oxidase

4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis

8-(3-Chlorostyryl)caffeine May Attenuate MPTP Neurotoxicity through Dual Actions of Monoamine Oxidase Inhibition and A2A Receptor Antagonism

8-Aryl- and alkyloxycaffeine analogues as inhibitors of monoamine oxidase

The adenosine A(2A) antagonistic properties of selected C8-substituted xanthines

The adenosine A2A antagonistic properties of selected C8-substituted xanthines

The adenosine receptor affinities and monoamine oxidase B inhibitory properties of sulfanylphthalimide analogues

α-Tetralone derivatives as inhibitors of monoamine oxidase

Azure B, a metabolite of methylene blue, is a high-potency, reversible inhibitor of monoamine oxidase

Azure B and a synthetic structural analogue of methylene blue, ethylthioninium chloride, present with antidepressant-like properties

Benzo[b]tiophen-3-ol derivatives as effective inhibitors of human monoamine oxidase: design, synthesis, and biological activity

Benzyloxynitrostyrene analogues – A novel class of selective and highly potent inhibitors of monoamine oxidase B

Betulin, a Newly Characterized Compound in Acacia auriculiformis Bark, Is a Multi-Target Protein Kinase Inhibitor

Caffeine as a lead compound for the design of therapeutic agents for the treatment of Parkinson's disease

Carbamate substituted 2-amino-4,6-diphenylpyrimidines as adenosine receptor antagonists

Chapter 5 - Multifunctional Enzyme Inhibition for Neuroprotection - A Focus on MAO, NOS, and AChE Inhibitors

Coumarin-Based Dual Inhibitors of Human Carbonic Anhydrases and Monoamine Oxidases Featuring Amino Acyl and ( Pseudo )-Dipeptidyl Appendages: In Vitro and Computational Studies

Coumarin derivatives as inhibitors of d-amino acid oxidase and monoamine oxidase

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