meta-Tiramin (m-tiramin, 3-tiramin, 3-hidroksifeniletilamin) je endogeno monoaminsko jedinjenje i trag amin iz klase fenetilamina.[4][5][6] On je pozicioni izomer para-tiramina, i slično njemu utiče na adrenergički i dopaminergiči sistem.[7][8]

meta-Tiramin
3-tyramine.png
IUPAC ime
Drugi nazivi m-Tiramin; 3-Tiramin; 3-Hidroksifeniletulamin
Identifikacija
CAS registarski broj 588-05-6
PubChem[1][2] 11492
ChemSpider[3] 11008
Jmol-3D slike Slika 1
Svojstva
Molekulska formula C8H11NO
Molarna masa 137.18 g mol−1



Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala

Infobox references

ReferenceUredi

  1. Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. http://www.sciencedirect.com/science/article/pii/S1359644610007737.  edit
  2. Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1. 
  3. Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. http://www.jcheminf.com/content/2/1/3.  edit
  4. Boulton AA, Huebert ND (November 1981). „Biosynthesis of some urinary trace amines in the rat and the human”. Research Communications in Chemical Pathology and Pharmacology 34 (2): 295–310. PMID 7335956. 
  5. Dyck LE, Juorio AV, Boulton AA (June 1982). „The in vitro release of endogenous m-tyramine, p-tyramine and dopamine from rat striatum”. Neurochemical Research 7 (6): 705–16. PMID 7121718. 
  6. Sardar A, Juorio AV, Boulton AA (June 1987). „The concentration of p- and m-tyramine in the rat mesolimbic system: its regional distribution and effect of monoamine oxidase inhibition”. Brain Research 412 (2): 370–4. DOI:10.1016/0006-8993(87)91145-0. PMID 3607473. http://linkinghub.elsevier.com/retrieve/pii/0006-8993(87)91145-0. 
  7. Dyck LE, Kazakoff CW, Dourish CT (October 1982). „The role of catecholamines, 5-hydroxytryptamine and m-tyramine in the behavioural effects of m-tyrosine in the rat”. European Journal of Pharmacology 84 (3-4): 139–49. DOI:10.1016/0014-2999(82)90196-0. PMID 7173317. 
  8. McQuade PS, Wood PL (1984). „The effects of administration of meta-tyramine and para-tyramine on dopamine and its metabolites in the rat striatum”. Progress in Neuro-psychopharmacology & Biological Psychiatry 8 (4-6): 705–9. PMID 6531442. 

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