Purinergic P1 Receptor Antagonists
"Purinergic P1 Receptor Antagonists" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Compounds that bind to and block the stimulation of PURINERGIC P1 RECEPTORS.
Descriptor ID |
D058915
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MeSH Number(s) |
D27.505.519.625.725.400.100 D27.505.696.577.725.400.100
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Concept/Terms |
Purinergic P1 Receptor Antagonists- Purinergic P1 Receptor Antagonists
- P1 Purinoceptor Antagonists
- Antagonists, P1 Purinoceptor
- Purinoceptor Antagonists, P1
- Adenosine Receptor Antagonists
- Antagonists, Adenosine Receptor
- Receptor Antagonists, Adenosine
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Below are MeSH descriptors whose meaning is more general than "Purinergic P1 Receptor Antagonists".
Below are MeSH descriptors whose meaning is more specific than "Purinergic P1 Receptor Antagonists".
This graph shows the total number of publications written about "Purinergic P1 Receptor Antagonists" by people in this website by year, and whether "Purinergic P1 Receptor Antagonists" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1994 | 0 | 3 | 3 | 1997 | 0 | 1 | 1 | 1998 | 0 | 1 | 1 | 2002 | 0 | 1 | 1 | 2013 | 1 | 1 | 2 |
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Below are the most recent publications written about "Purinergic P1 Receptor Antagonists" by people in Profiles.
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Vernall AJ, Stoddart LA, Briddon SJ, Ng HW, Laughton CA, Doughty SW, Hill SJ, Kellam B. Conversion of a non-selective adenosine receptor antagonist into A3-selective high affinity fluorescent probes using peptide-based linkers. Org Biomol Chem. 2013 Sep 14; 11(34):5673-82.
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Corriden R, Self T, Akong-Moore K, Nizet V, Kellam B, Briddon SJ, Hill SJ. Adenosine-A3 receptors in neutrophil microdomains promote the formation of bacteria-tethering cytonemes. EMBO Rep. 2013 Aug; 14(8):726-32.
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Hallworth R, Cato M, Colbert C, Rea MA. Presynaptic adenosine A1 receptors regulate retinohypothalamic neurotransmission in the hamster suprachiasmatic nucleus. J Neurobiol. 2002 Sep 05; 52(3):230-40.
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Haynes JM, Alexander SP, Hill SJ. A1 and A2 adenosine receptor modulation of contractility in the cauda epididymis of the guinea-pig. Br J Pharmacol. 1998 Oct; 125(3):570-6.
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Cooper J, Hill SJ, Alexander SP. An endogenous A2B adenosine receptor coupled to cyclic AMP generation in human embryonic kidney (HEK 293) cells. Br J Pharmacol. 1997 Oct; 122(3):546-50.
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Alexander SP, Curtis AR, Kendall DA, Hill SJ. A1 adenosine receptor inhibition of cyclic AMP formation and radioligand binding in the guinea-pig cerebral cortex. Br J Pharmacol. 1994 Dec; 113(4):1501-7.
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Peakman MC, Hill SJ. Adenosine A2B-receptor-mediated cyclic AMP accumulation in primary rat astrocytes. Br J Pharmacol. 1994 Jan; 111(1):191-8.
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Alexander SP, Losinski A, Kendall DA, Hill SJ. A comparison of A2 adenosine receptor-induced cyclic AMP generation in cerebral cortex and relaxation of pre-contracted aorta. Br J Pharmacol. 1994 Jan; 111(1):185-90.
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