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Key Documents

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SMB00019

Sigma-Aldrich

N-Acetyltyramine

≥95% (LC/MS-ELSD)

Sinónimos:

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

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About This Item

Fórmula empírica (notación de Hill):
C10H13NO2
Número de CAS:
1202-66-0
Peso molecular:
179.22
MDL number:
MFCD01670887
UNSPSC Code:
12352205
PubChem Substance ID:
329824672
NACRES:
NA.25

assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−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)

InChI key

ATDWJOOPFDQZNK-UHFFFAOYSA-N

Categorías relacionadas

General description

Natural product derived from fungal source.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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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
R G Macfarlane et al.
Journal of chromatography, 532(1), 13-25 (1990-10-26)
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 ionisation mass spectrometry (GC-NICIMS). Deuterium-labelled analogues of each compound were
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
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
Reversal of resistance by N-acetyltyramine or N-acetyl-2-phenylethylamine in doxorubicin-resistant leukemia P388 cells.
S Kunimoto et al.
The Journal of antibiotics, 40(11), 1651-1652 (1987-11-01)
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