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

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

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

http://www.wikidata.org/entity/Q28361938

about

Potent convulsant actions of the adenosine receptor antagonist, xanthine amine congener (XAC)FPL 66096: a novel, highly potent and selective antagonist at human platelet P2T-purinoceptors Further analysis of the mechanisms underlying the tracheal relaxant action of SCA40.1,3,8- and 1,3,7-substituted xanthines: relative potency as adenosine receptor antagonists at the frog neuromuscular junction Adenosine A1 and A2 receptors: structure--function relationships Cross talk between receptors mediating contraction and relaxation in the arterioles but not the dilator muscle of the rat iris.P2-purinoceptors mediating spasm of the isolated uterus of the non-pregnant guinea-pig.A comparison of A2 adenosine receptor-induced cyclic AMP generation in cerebral cortex and relaxation of pre-contracted aorta Contractions mediated by alpha 1-adrenoceptors and P2-purinoceptors in a cat colon circular muscle Subtypes of purinoceptors in rat and dog urinary bladder smooth muscles A2-purinoceptor-mediated relaxation in the guinea-pig coronary vasculature: a role for nitric oxide.Apparent affinity of 1,3-dipropyl-8-cyclopentylxanthine for adenosine A1 and A2 receptors in isolated tissues from guinea-pigs.A study of the purinoceptors mediating contraction in the rat colon.Effects of purines on the longitudinal muscle of the rat colon Characterization of the P1-purinoceptors mediating contraction of the rat colon muscularis mucosae.Characterization of P1-purinoceptors on rat duodenum and urinary bladder.Direct effects of adenylyl 5'-(beta,gamma-methylene)diphosphonate, a stable ATP analogue, on relaxant P1-purinoceptors in smooth muscle.Quantitative analysis of the agonist and antagonist actions of some ATP analogues at P2X-purinoceptors in the rabbit ear artery Characterization of adenosine receptors in guinea-pig isolated left atria.Effects of K(+)-channel blockers on A1-adenosine receptor-mediated negative inotropy and chronotropy of guinea-pig isolated left and right atria.Use of a newly developed technique to isolate rat pinealocytes and study the effects of adenosine agonists on melatonin production.Axon Outgrowth Is Regulated by an Intracellular Purine-sensitive Mechanism in Retinal Ganglion Cells

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P2860

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

http://www.wikidata.org/entity/Q28361938

description

1987 nî lūn-bûn

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1987 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

1987 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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1987年の論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年論文

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1987年论文

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name

Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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J.1476-5381.1987.TB11297.X

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British Journal of Pharmacology

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Apparent affinity of some 8-ph ...... in guinea-pig aorta and atria

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D M Tomkins

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K A Jacobson

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M G Collis

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P2860

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

Some quantitative uses of drug antagonists

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

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

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

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

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

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

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

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

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