N-Acetyltyramine
N-Acetyltyramine structure
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Common Name | N-Acetyltyramine | ||
|---|---|---|---|---|
| CAS Number | 1202-66-0 | Molecular Weight | 179.216 | |
| Density | 1.1±0.1 g/cm3 | Boiling Point | 424.1±28.0 °C at 760 mmHg | |
| Molecular Formula | C10H13NO2 | Melting Point | 134°C | |
| MSDS | Chinese USA | Flash Point | 210.3±24.0 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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Selective nanomolar detection of dopamine using a boron-doped diamond electrode modified with an electropolymerized sulfobutylether-beta-cyclodextrin-doped poly(N-acetyltyramine) and polypyrrole composite film.
Anal. Chem. 81(10) , 4089-98, (2009) N-acetyltyramine was synthesized and electropolymerized together with a negatively charged sulfobutylether-beta-cyclodextrin on a boron-doped diamond (BDD) electrode followed by the electropolymerization of pyrrole to form a stable and permselective film for ... |
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Mechanistic and structural analysis of Drosophila melanogaster arylalkylamine N-acetyltransferases.
Biochemistry 53(49) , 7777-93, (2014) Arylalkylamine N-acetyltransferase (AANAT) catalyzes the penultimate step in the biosynthesis of melatonin and other N-acetylarylalkylamides from the corresponding arylalkylamine and acetyl-CoA. The N-acetylation of arylalkylamines is a critical step in Droso... |
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Effect of acetyl derivatives of some sympathomimetic amines on the blood pressure of the rat.
Acta Pharmacol. Toxicol. (Copenh.) 40(2) , 247-58, (1977) The effect of five sympathomimetic amines and some of their acetyl derivatives on the blood pressure of the rat was determined on the left carotid artery. After pretreatment with chlorisondamine (1 mg/kg subcutaneously) the blood pressure rise by sympathomime... |
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Partial purification and properties of N-acetylhistamine deacetylase.
Biochim. Biophys. Acta 438(2) , 532-9, (1976) The enzyme catalyzing the deacetylaction of N-acetylhistamine was partially purified about 160-fold from rat liver extract and its properties were investigated. The purification procedure included DEAE-cellulose chromatography, precipitation with ammonium sul... |
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Effect of spores of saprophytic fungi on phytoalexin accumulation in seeds of frog-eye leaf spot and stem canker-resistant and -susceptible soybean (Glycine max L.) cultivars.
J. Agric. Food Chem. 48(8) , 3662-5, (2000) Two saprophytic fungi (Mucor ramosissimus and Rhizopus sp.) were tested for their ability to induce phytoalexin production by seeds of frog-eye leaf spot and stem canker-resistant and -susceptible soybean (Glycine max L.) cultivars. Only M. ramosissimus was s... |
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Changes in the content of brain biogenic amine associated with early colony establishment in the Queen of the ant, Formica japonica.
PLoS ONE 7(8) , e43377, (2012) We examined changes in the content of biogenic amines in the brains of ant queen associated with early colony establishment. In ants, including Formica japonica, winged virgin queens lose their wings following copulation, and then start establishing a colony.... |
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Identification and quantitation of N-acetyl metabolites of biogenic amines in the thoracic nervous system of the locust, Schistocerca gregaria, by gas chromatography-negative-ion chemical ionisation mass spectrometry.
J. Chromatogr. A. 532(1) , 13-25, (1990) The N-acetylated metabolites of p-tyramine, p-octopamine and dopamine were identified unambiguously and quantitatively determined in a single ventral thoracic nerve cord of the locust, Schistocerca gregaria, by gas chromatography-negative-ion chemical ionisat... |
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N-acylation of tyramines: purification and characterization of an arylamine N-acetyltransferase from rat brain and liver.
Can. J. Biochem. 57(10) , 1204-9, (1979) The N-acylation of tyramine isomers and other biogenic amines has been studied. The liver exhibits the highest activity towards tyramines, while the brain exhibits a low but significant activity. In the brain, tyramine N-acylation activity was heterogenously ... |
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Biosynthesis of N-acetyldopamine and N-acetyloctopamine by Schistocerca gregaria nervous tissue.
J. Neurochem. 36(2) , 441-6, (1981) N-Acetyltyramine, N-acetyldopamine and N-acetyloctopamine were the major products when either L-[3H]tyrosine or [3H]tyramine were incubated with thoracic ganglia of the desert locust, Schistocerca gregaria. No label was incorporated into L-DOPA under these co... |
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Reversal of resistance by N-acetyltyramine or N-acetyl-2-phenylethylamine in doxorubicin-resistant leukemia P388 cells.
J. Antibiot. 40(11) , 1651-2, (1987)
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