(Q28338174)

2

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T W Moody

3

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W Padgett

4

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E Pijl

5

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K L Kirk

6

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J W Daly

Journal of Medicinal Chemistry

7

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language of work or name

English

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publication date

August 1987

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published in

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volume

30

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issue

8

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page(s)

1529-32

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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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Functionalized congeners of adenosine: preparation of analogues with high affinity for A1-adenosine receptors

20 March 2017

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N6-functionalized congeners of adenosine with high potency at A2-adenosine receptors: potential ligands for affinity chromatography.

20 March 2017

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[3H]xanthine amine congener of 1,3-dipropyl-8-phenylxanthine: an antagonist radioligand for adenosine receptors

29 September 2017

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

29 September 2017

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

29 September 2017

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

29 September 2017

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Evidence that a novel 8-phenyl-substituted xanthine derivative is a cardioselective adenosine receptor antagonist in vivo

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An approach to the self regulatory mechanism of substance P actions: II. Biological activity of new synthetic peptide analogs related both to enkephalin and substance P.

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Stereostructure-activity relationship of opioid agonist and antagonist bivalent ligands. Evidence for bridging between vicinal opioid receptors

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Effects of (-)-N6-(R-phenylisopropyl)-adenosine (PIA) and caffeine on nociception and morphine-induced analgesia, tolerance and dependence in mice

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Arterial blood pressure response in conscious rabbits to administration of C-terminal fragment of substance P into the cerebral ventricles, intravenously and intragastrically

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Characterization of the antinociceptive effects of some adenosine analogues in the rat

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