Dual A1 and A2A adenosine receptor antagonists, methoxy substituted 2-benzylidene-1-indanone, suppresses intestinal postprandial glucose and attenuates hyperglycaemia in fructose-s... von Sanni, Olakunle, Terre'Blanche, Gisella

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Synthesis and Adenosine RA1/A2A Receptor Affinity of Selected Aurones and 2-Benzylidene-1-Indanones von van Rensburg, Helena D. Janse, Terre’Blanche, Gisella, Legoabe, Lesetja J.

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1,3,7-Triethyl-substituted xanthines—possess nanomolar affinity for the adenosine A1 receptor von Van der Walt, Mietha M., Terre’Blanche, Gisella

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On the basis of sex: male vs. female rat adenosine A1/A2A receptor affinity von Janse van Rensburg, Helena D, Terre'Blanche, Gisella, Van der Walt, Mietha M

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Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development von Matthee, Chrisna, Terre’Blanche, Gisella, Legoabe, Lesetja J., Janse van Rensburg, Helena D.

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Chalcone‐inspired rA1/A2A adenosine receptor ligands: Ring closure as an alternative to a reactive substructure von Matthee, Chrisna, Terre’Blanche, Gisella, Janse van Rensburg, Helena D., Aucamp, Janine, Legoabe, Lesetja J.

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New fused pyrroles with rA1/A2A antagonistic activity as potential therapeutics for neurodegenerative disorders von van Vuuren, Nadia Janse, van Rensburg, Helena D. Janse, Terre’Blanche, Gisella, Legoabe, Lesetja J.

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Correction to: Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development von Matthee, Chrisna, Terre’Blanche, Gisella, Legoabe, Lesetja J., van Rensburg, Helena D. Janse

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C3 amino-substituted chalcone derivative with selective adenosine rA1 receptor affinity in the micromolar range von Janse van Rensburg, Helena D., Legoabe, Lesetja J., Terre’Blanche, Gisella

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Benzyloxynitrostyrene analogues – A novel class of selective and highly potent inhibitors of monoamine oxidase B von Van der Walt, Mietha M., Terre’Blanche, Gisella, Petzer, Jacobus P., Petzer, Anél

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2-Aminopyrimidines as dual adenosine A1/A2A antagonists von Robinson, Sarel J., Petzer, Jacobus P., Terre’Blanche, Gisella, Petzer, Anél, van der Walt, Mietha M., Bergh, Jacobus J., Lourens, Anna C.U.

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Thio- and aminocaffeine analogues as inhibitors of human monoamine oxidase von Booysen, Hermanus P., Moraal, Christina, Terre’Blanche, Gisella, Petzer, Anél, Bergh, Jacobus J., Petzer, Jacobus P.

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Discovery of 1,3-diethyl-7-methyl-8-(phenoxymethyl)-xanthine derivatives as novel adenosine A 1 and A 2A receptor antagonists von Harmse, Rozanne, van der Walt, Mietha M, Petzer, Jacobus P, Terre'Blanche, Gisella

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Discovery of 1,3-diethyl-7-methyl-8-(phenoxymethyl)-xanthine derivatives as novel adenosine A1 and A2A receptor antagonists von Harmse, Rozanne, van der Walt, Mietha M., Petzer, Jacobus P., Terre’Blanche, Gisella

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Carbamate substituted 2-amino-4,6-diphenylpyrimidines as adenosine receptor antagonists von Robinson, Sarel J., Petzer, Jacobus P., Rousseau, Amanda L., Terre’Blanche, Gisella, Petzer, Anél, Lourens, Anna C.U.

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The adenosine A2A antagonistic properties of selected C8-substituted xanthines von Van der Walt, Mietha M., Terre’Blanche, Gisella, Petzer, Anél, Lourens, Anna C.U., Petzer, Jacobus P.

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The adenosine receptor affinities and monoamine oxidase B inhibitory properties of sulfanylphthalimide analogues von Van der Walt, Mietha M., Terre’Blanche, Gisella, Petzer, Anél, Petzer, Jacobus P.

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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... von Sanni, Olakunle, Terre'Blanche, Gisella

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Novel sulfanylphthalimide analogues as highly potent inhibitors of monoamine oxidase B von Van der Walt, Mietha M., Terre’Blanche, Gisella, Petzer, Anél, Petzer, Jacobus P.

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Evaluation of chemical constituents of Rooibos (Aspalathus linearis) and Honeybush (Cyclopia intermedia) as adenosine A1/A2A receptor ligands von Gouws, Liezel, Janse van Rensburg, Helena D., Terre’Blanche, Gisella, Van der Walt, Mietha M.

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