Aminopyridines
"Aminopyridines" 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.
Pyridines substituted in any position with an amino group. May be hydrogenated, but must retain at least one double bond.
Descriptor ID |
D000631
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MeSH Number(s) |
D02.092.080 D03.383.725.050
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Aminopyridines".
Below are MeSH descriptors whose meaning is more specific than "Aminopyridines".
This graph shows the total number of publications written about "Aminopyridines" by people in this website by year, and whether "Aminopyridines" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1981 | 3 | 1 | 4 | 1983 | 1 | 0 | 1 | 1984 | 0 | 1 | 1 | 1989 | 0 | 1 | 1 | 2013 | 1 | 0 | 1 | 2014 | 1 | 0 | 1 | 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Aminopyridines" by people in Profiles.
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Forkuo GS, Kim H, Thanawala VJ, Al-Sawalha N, Valdez D, Joshi R, Parra S, Pera T, Gonnella PA, Knoll BJ, Walker JK, Penn RB, Bond RA. Phosphodiesterase 4 Inhibitors Attenuate the Asthma Phenotype Produced by ß2-Adrenoceptor Agonists in Phenylethanolamine N-Methyltransferase-Knockout Mice. Am J Respir Cell Mol Biol. 2016 Aug; 55(2):234-42.
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Mohedas AH, Wang Y, Sanvitale CE, Canning P, Choi S, Xing X, Bullock AN, Cuny GD, Yu PB. Structure-activity relationship of 3,5-diaryl-2-aminopyridine ALK2 inhibitors reveals unaltered binding affinity for fibrodysplasia ossificans progressiva causing mutants. J Med Chem. 2014 Oct 09; 57(19):7900-15.
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Sanvitale CE, Kerr G, Chaikuad A, Ramel MC, Mohedas AH, Reichert S, Wang Y, Triffitt JT, Cuny GD, Yu PB, Hill CS, Bullock AN. A new class of small molecule inhibitor of BMP signaling. PLoS One. 2013; 8(4):e62721.
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Alkadhi KA, Hogan YH. Effect of calcium on synaptic facilitation by potassium channel blockers in superior cervical ganglion of rat. Neuropharmacology. 1989 Jan; 28(1):75-81.
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Alkadhi KA, Brown TR, Sabouni MH. Inhibitory effect of adenosine on transmission in sympathetic ganglia. Naunyn Schmiedebergs Arch Pharmacol. 1984 Nov; 328(1):16-9.
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Hadfield AJ, Robinson NR, Hill SJ. The nature of the binding of [3H]mepyramine to homogenates of guinea-pig cerebral cortex at different [3H]ligand concentrations. Biochem Pharmacol. 1983 Aug 15; 32(16):2449-51.
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Hill SJ, Daum P, Young JM. Affinities of histamine H1-antagonists in guinea pig brain: similarity of values determined from [3H]mepyramine binding and from inhibition of a functional response. J Neurochem. 1981 Nov; 37(5):1357-60.
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Volle RL, Quenzer LF, Patterson BA, Alkadhi KA, Henderson EG. Cyclic guanosine 3':5'-monophosphate accumulation and 45Ca-uptake by rat superior cervical ganglia during preganglionic stimulation. J Pharmacol Exp Ther. 1981 Nov; 219(2):338-43.
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Hill SJ, Hiley CR, Young JM. Extended mepyramine treatment and histamine H1-receptors in guinea-pig brain. Eur J Pharmacol. 1981 May 22; 71(4):421-8.
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Hill SJ, Young JM. Characterization of [3H]mepyramine binding to the longitudinal muscle of guinea pig small intestine. Mol Pharmacol. 1981 May; 19(3):379-87.
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