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SMB00019

Sigma-Aldrich

N-Acetyltyramine

≥95% (LC/MS-ELSD)

Synonym(e):

N-(2-(4-Hydroxyphenyl)ethyl)acetamide, N-(p-Hydroxyphenethyl)acetamide, N-Acetyl tyramine

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About This Item

Empirische Formel (Hill-System):
C10H13NO2
CAS-Nummer:
1202-66-0
Molekulargewicht:
179.22
MDL-Nummer:
MFCD01670887
UNSPSC-Code:
12352205
PubChem Substanz-ID:
329824672
NACRES:
NA.25

Assay

≥95% (LC/MS-ELSD)

Form

solid

Anwendung(en)

metabolomics
vitamins, nutraceuticals, and natural products

Lagertemp.

−20°C

InChI

1S/C10H13NO2/c1-8(12)11-7-6-9-2-4-10(13)5-3-9/h2-5,13H,6-7H2,1H3,(H,11,12)

InChIKey

ATDWJOOPFDQZNK-UHFFFAOYSA-N

Verwandte Kategorien

Allgemeine Beschreibung

Natural product derived from fungal source.

Piktogramme

Corrosion
GHS05

Signalwort

Danger

H-Sätze

H318

Gefahreneinstufungen

Eye Dam. 1

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

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S Friström et al.
Acta pharmacologica et toxicologica, 40(2), 247-258 (1977-02-01)
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 sympathomimetic amines
A K Mir et al.
Journal of neurochemistry, 36(2), 441-446 (1981-02-01)
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 conditions, although 2-3% of the radioactivity could be
W S Garcez et al.
Journal of agricultural and food chemistry, 48(8), 3662-3665 (2000-08-24)
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 shown to elicit
P H Yu et al.
Canadian journal of biochemistry, 57(10), 1204-1209 (1979-10-01)
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 distributed. The arylamine
Fengjun Shang et al.
Analytical chemistry, 81(10), 4089-4098 (2009-04-23)
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 selective dopamine detection. The selectivity and sensitivity of the
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