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MilliporeSigma

M0257

Sigma-Aldrich

Methyl N-acetyl-α-D-glucosaminide

Sinónimos:

Methyl 2-acetamido-2-deoxy-α-D-glucopyranoside

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About This Item

Fórmula empírica (notación de Hill):
C9H17NO6
Número de CAS:
Peso molecular:
235.23
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:

biological source

synthetic (organic)

assay

≥98%

form

powder

storage temp.

2-8°C

SMILES string

CO[C@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1NC(C)=O

InChI

1S/C9H17NO6/c1-4(12)10-6-8(14)7(13)5(3-11)16-9(6)15-2/h5-9,11,13-14H,3H2,1-2H3,(H,10,12)/t5-,6-,7-,8-,9+/m1/s1

InChI key

ZEVOCXOZYFLVKN-OKNNCHMLSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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R Zeitler et al.
European journal of biochemistry, 204(3), 1165-1168 (1992-03-15)
During the search for inhibitors of N-acetylneuraminic acid biosynthesis, it was shown that 3-O-methyl-N-acetylglucosamine competitively inhibits the N-acetylglucosamine kinase of rat liver in vitro with a Ki value of 17 microM. N-Acetylmannosamine kinase is inhibited non-competitively with a Ki value
I Miwa et al.
Enzyme & protein, 48(3), 135-142 (1994-01-01)
Glucokinase, an enzyme that catalyzes the phosphorylation of glucose, constitutes the key regulatory step in glucose metabolism in pancreatic islets and liver. We found that 3-O-methyl-N-acetyl-D-glucosamine (3-O-methyl-GlcNAc) potently inhibits glucose phosphorylation by N-acetylglucosamine kinase whereas glucokinase is not at all
M E Etzler et al.
The Journal of biological chemistry, 256(5), 2367-2370 (1981-03-10)
Equilibrium dialysis studies on the binding of the Dolichos biflorus lectin with [14C]methyl alpha-D-GalNAc showed that the lectin has two combining sites/molecule and an intrinsic association constant at 3 degrees C of 4.2 X 10(3) liters mol-1. Binding studies on
S Araki et al.
The Journal of biological chemistry, 262(29), 14141-14145 (1987-10-15)
A novel phosphonoglycosphingolipid named SGL-I containing 3 mol of 2-aminoethylphosphonate residues was isolated from the skin of a sea gastropod, Aplysia kurodai. The saccharide moiety of the glycolipid was characterized as 4-O-methyl-GlcNAc alpha 1----4GalNAc alpha-1----3 [6'-O-(2-aminoethylphosphonyl)Gal alpha 1----2] (2-aminoethylphosphonyl----6)Gal beta
Gas--liquid chromatography and mass spectrometry of methylated and acetylated methyl glycosides. Application to the structural analysis of glycoprotein glycans.
B Fournet et al.
Analytical biochemistry, 116(2), 489-502 (1981-09-15)

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