(Q28361938)

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Apparent affinity of some 8-phenyl-substituted xanthines at adenosine receptors in guinea-pig aorta and atria

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Apparent affinity of some 8-phenyl-substituted xanthines at adenosine receptors in guinea-pig aorta and atria (English)

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M G Collis

1

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K A Jacobson

series ordinal

2

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D M Tomkins

series ordinal

3

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language of work or name

English

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publication date

September 1987

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published in

British Journal of Pharmacology

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volume

92

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page(s)

69-75

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issue

1

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cites work

Functionalized congeners of 1,3-dipropyl-8-phenylxanthine: potent antagonists for adenosine receptors that modulate membrane adenylate cyclase in pheochromocytoma cells, platelets and fat cells

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PubMed Central

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20 March 2017

Some quantitative uses of drug antagonists

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7 April 2017

Species differences in structure-activity relationships of adenosine agonists and xanthine antagonists at brain A1 adenosine receptors

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PubMed Central

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29 September 2017

A functionalized congener approach to adenosine receptor antagonists: amino acid conjugates of 1,3-dipropylxanthine

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PubMed Central

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29 September 2017

A novel 8-phenyl-substituted xanthine derivative is a selective antagonist at adenosine A1-receptors in vivo

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PubMed Central

reference URL

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29 September 2017

Functionalized congeners of 1,3-dialkylxanthines: preparation of analogues with high affinity for adenosine receptors

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PubMed Central

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29 September 2017

PACPX--a substituted xanthine--antagonizes both the A1 and A2 subclasses of the P1-purinoceptor: antagonism of the A2 subclass is competitive but antagonism of the A1 subclass is not

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PubMed Central

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29 September 2017

Adenosine regulates via two different types of receptors, the accumulation of cyclic AMP in cultured brain cells

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The relative contribution of affinity and efficacy to agonist activity: organ selectivity of noradrenaline and oxymetazoline with reference to the classification of drug receptors

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2 June 2018

Structure-activity relationships for N6-substituted adenosines at a brain A1-adenosine receptor with a comparison to an A2-adenosine receptor regulating coronary blood flow.

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2 June 2018

1,3-Dialkyl-8-(p-sulfophenyl)xanthines: potent water-soluble antagonists for A1- and A2-adenosine receptors

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2 June 2018

Comparison of the potency of 8-phenyltheophylline as an antagonist at A1 and A2 adenosine receptors in atria and aorta from the guinea-pig

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2 June 2018

On the mechanism of activation of muscarinic K+ channels by adenosine in isolated atrial cells: involvement of GTP-binding proteins

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2 June 2018

The Uptake of Atropine and Related Drugs by Intestinal Smooth Muscle of the Guinea-Pig in Relation to Acetylcholine Receptors

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Crossref

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https://api.crossref.org/works/10.1111%2FJ.1476-5381.1987.TB11297.X

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21 January 2018

Adenosine relaxes the aorta by interacting with an A2 receptor and an intracellular site

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3664093

retrieved

12 December 2020

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inferred from PubMed ID database lookup

2-Chloroadenosine, a permeant for the nucleoside transporter

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3664093

retrieved

12 December 2020

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Identifiers

DOI

10.1111/J.1476-5381.1987.TB11297.X

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release_k647ptbnbjcvbgfqqxinbwxafy

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24 November 2022

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ResearchGate publication ID

19498028

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(Q28361938)

Apparent affinity of some 8-phenyl-substituted xanthines at adenosine receptors in guinea-pig aorta and atria

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