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T3879

Sigma-Aldrich

L-Tyrosinamide

≥98% (TLC)

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About This Item

Formule empirique (notation de Hill):
C9H12N2O2
Numéro CAS:
4985-46-0
Poids moléculaire :
180.20
Numéro MDL:
MFCD00069935
Code UNSPSC :
12352209
ID de substance PubChem :
24900175
Nomenclature NACRES :
NA.26

product name

L-Tyrosinamide,

Pureté

≥98% (TLC)

Forme

powder

Couleur

white to off-white

Chaîne 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

Clé InChI

PQFMNVGMJJMLAE-QMMMGPOBSA-N

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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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