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Documentos Principais

A0167

Sigma-Aldrich

Galacto-N-biose

Sinônimo(s):

β-D-Gal-(1→3)-D-GalNAc, 2-Acetamido-2-deoxy-3-O-β-D-galactopyranosyl-D-galactopyranose, T Antigen

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About This Item

Fórmula empírica (Notação de Hill):
C14H25NO11
Número CAS:
20972-29-6
Peso molecular:
383.35
Número MDL:
MFCD00063995
Código UNSPSC:
12352201
ID de substância PubChem:
24890406
NACRES:
NA.25

Ensaio

≥98% (TLC)

Formulário

powder

técnica(s)

thin layer chromatography (TLC): suitable

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@H](O)[C@@H]1O[C@@H]2O[C@H](CO)[C@H](O)[C@H](O)[C@H]2O

InChI

1S/C14H25NO11/c1-4(18)15-7-12(9(20)6(3-17)24-13(7)23)26-14-11(22)10(21)8(19)5(2-16)25-14/h5-14,16-17,19-23H,2-3H2,1H3,(H,15,18)/t5-,6-,7-,8+,9+,10+,11-,12-,13-,14+/m1/s1

chave InChI

HMQPEDMEOBLSQB-UFLFEMAHSA-N

Aplicação

Galacto-N-biose, a component of the galacto-N-biose/lacto-N-biose metabolic pathway, is used as a substrate to identify, differentiate and characterize enzymes such as N-acetylglucosaminyltransferase(s), fucosyl- and sialyltransferase(s), galactosidase(s) and galacto-N-biose/lacto-N-biose I phosphorylase(s) (GLNBP). Galacto-N-biose is used in lectin inhibition studies.

Substratos

A substrate for N-acetylglucosaminyltransferase, fucosyl- and sialyltransferase, and galactosidase. Also used in lectin inhibition studies.

Outras notas

To gain a comprehensive understanding of our extensive range of Disaccharides for your research, we encourage you to visit our Carbohydrates Category page.

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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Certificados de análise (COA)

Lot/Batch Number
109K5012V
110M4009V
091M4012V
087H51135
087H51134

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6′-Sialyl-D-lactose Na salt, ≥98.0% (HPLC)

Sigma-Aldrich

40817

6′-Sialyl-D-lactose

D-(+)-Raffinose pentahydrate analytical standard

Supelco

95068

D-(+)-Raffinose pentahydrate

D Williams et al.
The Journal of biological chemistry, 255(23), 11253-11261 (1980-12-10)
The preceding paper (Williams, D., and Schachter, H. (1980) J. Biol. Chem. 255, 0000-0000) described a novel N-acetylglucosaminyltransferase in canine submaxillary gland microsomes which catalyzed the incorporation of GlcNAc into mucin acceptors. We show in the present report that the
T A Beyer et al.
The Journal of biological chemistry, 255(11), 5373-5379 (1980-06-10)
The acceptor substrate specificity and kinetic properties of the purified porcine submaxillary beta-galactoside alpha 1 leads to 2 fucosyltransferase have been examined. The transferase forms the Fuc alpha 1 leads to 2Gal linkage with oligosaccharides, glycoproteins, and glycolipids which contain
S E Tollefsen et al.
The Journal of biological chemistry, 258(8), 5172-5176 (1983-04-25)
We have examined the carbohydrate binding specificity of the B4 lectin from Vicia villosa seeds. The B4 lectin agglutinates Tn-exposed erythrocytes specifically and binds to these erythrocytes (1.4 X 10(6) sites/cell) with an association constant of 4.2 X 10(7) M-1.
D M Moujalled et al.
Cell death & disease, 4, e465-e465 (2013-01-19)
Ligation of tumor necrosis factor receptor 1 (TNFR1) can cause cell death by caspase 8 or receptor-interacting protein kinase 1 (RIPK1)- and RIPK3-dependent mechanisms. It has been assumed that because RIPK1 bears a death domain (DD), but RIPK3 does not
J I Rearick et al.
The Journal of biological chemistry, 254(11), 4444-4451 (1979-06-10)
The substrate requirements, linkage specificity, and kinetic mechanism of a pure sialyltransferase from porcine submaxillary glands have been examined. The enzyme transfers sialic acid from the donor nucleotide, CMP-NeuAc, into the sequence NeuAcalpha2 leads to 3Galbeta1 leads to 3GalNAc, which
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