(Q28378974)

1

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E Ongini

2

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C Zocchi

3

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G Arslan

5

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B B Fredholm

British Journal of Pharmacology

6

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language of work or name

English

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publication date

June 1997

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published in

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volume

121

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issue

3

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page(s)

353-60

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cites work

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Binding of the radioligand [3H]-SCH 58261, a new non-xanthine A2A adenosine receptor antagonist, to rat striatal membranes

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Binding of the novel nonxanthine A2A adenosine receptor antagonist [3H]SCH58261 to coronary artery membranes

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7 January 2021

PD 115,199: an antagonist ligand for adenosine A2 receptors.

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2-Alkynyl derivatives of adenosine and adenosine-5'-N-ethyluronamide as selective agonists at A2 adenosine receptors

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Evidence for high-affinity binding sites for the adenosine A2A receptor agonist [3H] CGS 21680 in the rat hippocampus and cerebral cortex that are different from striatal A2A receptors.

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Molecular characterization of a human brain adenosine A2 receptor

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G proteins: transducers of receptor-generated signals

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Effects of mono- and divalent ions on the binding of the adenosine analogue CGS 21680 to adenosine A2 receptors in rat striatum

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The binding of the adenosine A2 receptor selective agonist [3H]CGS 21680 to rat cortex differs from its binding to rat striatum

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The selective adenosine A2A receptor antagonist SCH 58261 discriminates between two different binding sites for [3H]-CGS 21680 in the rat brain.

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LIGAND: A versatile computerized approach for characterization of ligand-binding systems

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A modification of a protein-binding method for rapid quantification of cAMP in cell-culture supernatants and body fluid

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Autoradiographic evidence for G-protein coupled A2-receptors in rat neostriatum using [3H]-CGS 21680 as a ligand

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Functional characterization of adenosine A2 receptors in Jurkat cells and PC12 cells using adenosine receptor agonists.

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Binding characteristics of the adenosine A2 receptor ligand [3H]CGS 21680 to human platelet membranes

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