SMB00019
N-Acetyltyramine
≥95% (LC/MS-ELSD)
别名:
N-(2-(4-Hydroxyphenyl)ethyl)acetamide, N-(p-Hydroxyphenethyl)acetamide, N-Acetyl tyramine
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关于此项目
经验公式（希尔记法）:
C10H13NO2
化学文摘社编号:
分子量:
179.22
UNSPSC Code:
12352205
PubChem Substance ID:
NACRES:
NA.25
MDL number:
产品名称
N-Acetyltyramine, ≥95% (LC/MS-ELSD)
SMILES string
N(CCc1ccc(cc1)O)C(=O)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
assay
≥95% (LC/MS-ELSD)
form
solid
application(s)
metabolomics
vitamins, nutraceuticals, and natural products
storage temp.
−20°C
General description
Natural product derived from fungal source.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
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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