meta-Tyramine
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| Names | |
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| IUPAC name
3-(2-Aminoethyl)phenol
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| Other names
m-Tyramine; 3-Tyramine; 3-Hydroxyphenylethylamine
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| Identifiers | |
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3D model (Jmol)
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| ChemSpider | |
| ECHA InfoCard | 100.197.155 |
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PubChem CID
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| Properties | |
| C8H11NO | |
| Molar mass | 137.18 g·mol−1 |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
meta-Tyramine, also known as m-tyramine or 3-tyramine as well as 3-hydroxyphenylethylamine, is an endogenous monoamine compound and trace amine of the phenethylamine class.[1][2][3] It is a positional isomer of para-tyramine, and similarly to it, has effects on the adrenergic and dopaminergic systems.[4][5]
See also[edit]
References[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. doi:10.1007/bf00965523. 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. doi:10.1016/0278-5846(84)90042-3. PMID 6531442.
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