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T3879

Sigma-Aldrich

L-Tyrosinamide

≥98% (TLC)

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About This Item

Fórmula empírica (Notação de Hill):
C9H12N2O2
Número CAS:
Peso molecular:
180.20
Número MDL:
Código UNSPSC:
12352209
ID de substância PubChem:
NACRES:
NA.26

product name

L-Tyrosinamide,

Ensaio

≥98% (TLC)

forma

powder

cor

white to off-white

cadeia de caracteres SMILES

N[C@@H](Cc1ccc(O)cc1)C(N)=O

InChI

1S/C9H12N2O2/c10-8(9(11)13)5-6-1-3-7(12)4-2-6/h1-4,8,12H,5,10H2,(H2,11,13)/t8-/m0/s1

chave InChI

PQFMNVGMJJMLAE-QMMMGPOBSA-N

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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Cosmin Stefan Mocanu et al.
Molecules (Basel, Switzerland), 25(19) (2020-10-08)
Aluminium (Al) is clearly neurotoxic and considerable evidence exists that Al may play a role in the aetiology or pathogenesis of Alzheimer's disease (AD). Nevertheless, the link between AD pathology and Al is still open to debate. Therefore, we investigated
Po-Hsun Lin et al.
The journal of physical chemistry. B, 112(21), 6665-6673 (2008-05-07)
In recent years, several high-resolution structures of aptamer complexes have shed light on the binding mode and recognition principles of aptamer complex interactions. In some cases, however, the aptamer complex binding behavior and mechanism are not clearly understood, especially with
Josephine Ruta et al.
Analytical chemistry, 81(17), 7468-7473 (2009-07-28)
In this paper, a new fluorescence polarization (FP) assay strategy is described reporting the first demonstration of a noncompetitive FP technique dedicated to the small molecule sensing. This approach was based on the unique induced-fit binding mechanism of nucleic acid
Caroline Descôteaux et al.
Steroids, 77(5), 403-412 (2012-01-10)
L-para-Tyrosine was linked to ortho-hydroxyaniline, meta-hydroxyaniline and para-hydroxyaniline giving three distinct tyrosinamide molecules. The new extended amino acid derivatives were constructed to imitate, in part, the estradiol (E(2), the natural female sex hormone) nucleus. The resulting tyrosinamides were then linked
M L Corradi Da Silva et al.
Archives of biochemistry and biophysics, 318(2), 465-475 (1995-04-20)
A library of 15 N-linked oligosaccharide structures was prepared from ovalbumin and characterized using high-field NMR and mass spectrometry. The oligosaccharides were enzymatically released from ovalbumin glycopeptides, and the reducing ends were reacted with ammonium bicarbonate to form oligosaccharide-glycosylamines. These

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