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Dual A1 and A2A adenosine receptor antagonists, methoxy substituted 2-benzylidene-1-indanone, suppresses intestinal postprandial glucose and attenuates hyperglycaemia in fructose-streptozotocin diabetic rats

BMC endocrine disorders, 2023-05, Vol.23 (1), p.1-97, Article 97

2023

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Insight into the mechanism and toxicology of nitrofurantoin: a metabolomics approach

Drug and chemical toxicology (New York, N.Y. 1978), 2023-11, p.1-10

2023

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Synthesis and Adenosine RA1/A2A Receptor Affinity of Selected Aurones and 2-Benzylidene-1-Indanones

Pharmaceutical chemistry journal, 2023-08, Vol.57 (5), p.729-734

2023

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1,3,7-Triethyl-substituted xanthines—possess nanomolar affinity for the adenosine A1 receptor

Bioorganic & medicinal chemistry, 2015-10, Vol.23 (20), p.6641-6649

2015

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On the basis of sex: male vs. female rat adenosine A1/A2A receptor affinity

BMC research notes, 2023-08, Vol.16 (1), p.1-165, Article 165

2023

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Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development

Molecular diversity, 2022-06, Vol.26 (3), p.1779-1821

2022

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Chalcone‐inspired rA1/A2A adenosine receptor ligands: Ring closure as an alternative to a reactive substructure

Chemical biology & drug design, 2022-03, Vol.99 (3), p.416-437

2022

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New fused pyrroles with rA1/A2A antagonistic activity as potential therapeutics for neurodegenerative disorders

Molecular diversity, 2022-08, Vol.26 (4), p.2211-2220

2022

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Correction to: Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development

Molecular diversity, 2022-08, Vol.26 (4), p.2371-2371

2022

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C3 amino-substituted chalcone derivative with selective adenosine rA1 receptor affinity in the micromolar range

Chemical papers, 2021, Vol.75 (4), p.1581-1605

2021

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2-Benzylidene-1-Indanone Analogues as Dual Adenosine A1/A2a Receptor Antagonists for the Potential Treatment of Neurological Conditions

Drug research, 2019-07, Vol.69 (7), p.382

2019

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Synthesis and Structure Activity Relationships of Chalcone based Benzocycloalkanone Derivatives as Adenosine A1 and/or A2A Receptor Antagonists

Drug research, 2020-06, Vol.70 (6), p.243

2020

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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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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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Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase

Bioorganic & medicinal chemistry, 2011-12, Vol.19 (24), p.7507-7518

2011

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Discovery of 1,3-diethyl-7-methyl-8-(phenoxymethyl)-xanthine derivatives as novel adenosine A1 and A2A receptor antagonists

Bioorganic & medicinal chemistry letters, 2016-12, Vol.26 (24), p.5951-5955

2016

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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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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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Dual A 1 and A 2A adenosine receptor antagonists, methoxy substituted 2-benzylidene-1-indanone, suppresses intestinal postprandial glucose and attenuates hyperglycaemia in fructose-streptozotocin diabetic rats

BMC endocrine disorders, 2023-05, Vol.23 (1), p.97

2023

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Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B

Bioorganic & medicinal chemistry letters, 2012-11, Vol.22 (21), p.6632-6635

2012

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Evaluation of chemical constituents of Rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia) as adenosine A1/A2A receptor ligands

Medicinal chemistry research, 2023-12, Vol.32 (12), p.2535-2548

2023

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Inhibition of monoamine oxidase B by selected benzimidazole and caffeine analogues

Bioorganic & medicinal chemistry, 2007-06, Vol.15 (11), p.3692-3702

2007

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Sulfanylphthalonitrile analogues as selective and potent inhibitors of monoamine oxidase B

Bioorganic & medicinal chemistry letters, 2012-12, Vol.22 (24), p.7367-7370

2012

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Design, synthesis and evaluation of amino-3,5-dicyanopyridines and thieno[2,3-b]pyridines as ligands of adenosine A1 receptors for the potential treatment of epilepsy

Medicinal chemistry research, 2022, Vol.31 (8), p.1277-1297

2022

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Dual A1 and A2A adenosine receptor antagonists, methoxy substituted 2-benzylidene-1-indanone, suppresses intestinal postprandial glucose and attenuates hyperglycaemia in fructose-streptozotocin diabetic rats

Insight into the mechanism and toxicology of nitrofurantoin: a metabolomics approach

Synthesis and Adenosine RA1/A2A Receptor Affinity of Selected Aurones and 2-Benzylidene-1-Indanones

1,3,7-Triethyl-substituted xanthines—possess nanomolar affinity for the adenosine A1 receptor

On the basis of sex: male vs. female rat adenosine A1/A2A receptor affinity

Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development

Chalcone‐inspired rA1/A2A adenosine receptor ligands: Ring closure as an alternative to a reactive substructure

New fused pyrroles with rA1/A2A antagonistic activity as potential therapeutics for neurodegenerative disorders

Correction to: Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development

C3 amino-substituted chalcone derivative with selective adenosine rA1 receptor affinity in the micromolar range

2-Benzylidene-1-Indanone Analogues as Dual Adenosine A1/A2a Receptor Antagonists for the Potential Treatment of Neurological Conditions

Synthesis and Structure Activity Relationships of Chalcone based Benzocycloalkanone Derivatives as Adenosine A1 and/or A2A Receptor Antagonists

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

2-Aminopyrimidines as dual adenosine A1/A2A antagonists

Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase

Discovery of 1,3-diethyl-7-methyl-8-(phenoxymethyl)-xanthine derivatives as novel adenosine A1 and A2A receptor antagonists

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

The adenosine A2A antagonistic properties of selected C8-substituted xanthines

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

Dual A 1 and A 2A adenosine receptor antagonists, methoxy substituted 2-benzylidene-1-indanone, suppresses intestinal postprandial glucose and attenuates hyperglycaemia in fructose-streptozotocin diabetic rats

Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B

Evaluation of chemical constituents of Rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia) as adenosine A1/A2A receptor ligands

Inhibition of monoamine oxidase B by selected benzimidazole and caffeine analogues

Sulfanylphthalonitrile analogues as selective and potent inhibitors of monoamine oxidase B

Design, synthesis and evaluation of amino-3,5-dicyanopyridines and thieno[2,3-b]pyridines as ligands of adenosine A1 receptors for the potential treatment of epilepsy

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