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
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IUPAC ime
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Drugi nazivi
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m-Tiramin; 3-Tiramin; 3-Hidroksifeniletulamin
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Identifikacija
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CAS registarski broj
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588-05-6
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PubChem[1][2]
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11492
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ChemSpider[3]
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11008
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Jmol-3D slike
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Slika 1
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InChI=1S/C8H11NO/c9-5-4-7-2-1-3-8(10)6-7/h1-3,6,10H,4-5,9H2 Y Kod: GHFGJTVYMNRGBY-UHFFFAOYSA-N Y
InChI=InChI=1S/C8H11NO/c9-5-4-7-2-1-3-8(10)6-7/h1-3,6,10H,4-5,9H2 |
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Svojstva
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Molekulska formula
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C8H11NO
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Molarna masa
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137.18 g mol−1
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Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
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Infobox references
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- ↑ 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. edit
- ↑ 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.
- ↑ 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. edit
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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.
- ↑ 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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