(Q48096397)

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Autoradiographic comparison of the potency of several structurally unrelated adenosine receptor antagonists at adenosine A1 and A(2A) receptors.

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

Autoradiographic comparison of the potency of several structurally unrelated adenosine receptor antagonists at adenosine A1 and A(2A) receptors. (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

author name string

Fredholm BB

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

Lindström K

2

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

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publication date

1 September 1999

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

European Journal of Pharmacology

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

380

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

2-3

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

197-202

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Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

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1 reference

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Regional differences in the effect of guanine nucleotides on agonist and antagonist binding to adenosine A1-receptors in rat brain, as revealed by autoradiography.

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Purinoceptors in the nervous system.

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[3H]SCH 58261, a selective adenosine A2A receptor antagonist, is a useful ligand in autoradiographic studies.

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Structure-activity relationships of 8-styrylxanthines as A2-selective adenosine antagonists

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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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Comparative pharmacology of human adenosine receptor subtypes - characterization of stably transfected receptors in CHO cells.

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KF17837 ((E)-8-(3,4-dimethoxystyryl)-1,3-dipropyl-7-methylxanthine), a potent and selective adenosine A2 receptor antagonist

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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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Magnesium-Dependent Enhancement of Endogenous Agonist Binding to A1Adenosine Receptors: A Complicating Factor in Quantitative Autoradiography

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The in vitro pharmacology of ZM 241385, a potent, non‐xanthine, A2a selective adenosine receptor antagonist

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4-Amino[1,2,4]triazolo[4,3-a]quinoxalines. A novel class of potent adenosine receptor antagonists and potential rapid-onset antidepressants.

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(E)-1,3-Dialkyl-7-methyl-8-(3,4,5-trimethoxystyryl)xanthines: potent and selective adenosine A2 antagonists

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Cellular expression of adenosine A2A receptor messenger RNA in the rat central nervous system with special reference to dopamine innervated areas.

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The stimulatory action and the development of tolerance to caffeine is associated with alterations in gene expression in specific brain regions.

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7 January 2021

Identifiers

10.1016/S0014-2999(99)00533-6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/10513579

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