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Merck
모든 사진(1)

주요 문서

SMB00019

Sigma-Aldrich

N-Acetyltyramine

≥95% (LC/MS-ELSD)

동의어(들):

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

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About This Item

실험식(Hill 표기법):
C10H13NO2
CAS Number:
Molecular Weight:
179.22
MDL number:
UNSPSC 코드:
12352205
PubChem Substance ID:
NACRES:
NA.25
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분석

≥95% (LC/MS-ELSD)

양식

solid

응용 분야

metabolomics
vitamins, nutraceuticals, and natural products

저장 온도

−20°C

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

일반 설명

Natural product derived from fungal source.

픽토그램

Corrosion

신호어

Danger

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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시험 성적서(COA)

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문서 라이브러리 방문

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
Y Endo
Biochimica et biophysica acta, 438(2), 532-539 (1976-07-08)
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 sulfate and DEAE-cellulose rechromatography. The enzyme contains a labile -SH
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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