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Merck
CN

49095

2-Acetamido-2-deoxy-6-O-(α-L-fucopyranosyl)-D-glucopyranose

≥98.0% (TLC)

别名:

2-Acetamido-2-deoxy-6-O-(6-deoxy-α-L-galactopyranosyl)-D-glucopyranose, Fucosyl-α-1,6-N-acetylglucosamine

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关于此项目

经验公式(希尔记法):
C14H25NO10
分子量:
367.35
PubChem Substance ID:
UNSPSC Code:
12352200
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assay

≥98.0% (TLC)

storage temp.

−20°C

SMILES string

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

InChI

1S/C14H25NO10/c1-4-8(17)11(20)12(21)14(24-4)23-3-6-9(18)10(19)7(13(22)25-6)15-5(2)16/h4,6-14,17-22H,3H2,1-2H3,(H,15,16)/t4?,6?,7-,8+,9+,10?,11?,12+,13+,14+/m0/s1

InChI key

BSNVYGSAFLBSSQ-ZXPKOIJOSA-N

Application

Disaccharide for testing alpha-1,6-fucosylation of N-acetylglucosamine

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

新产品

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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N Kojima et al.
Journal of biochemistry, 124(4), 726-737 (1998-10-02)
To determine the effect of alpha1,6-linked fucose modification of N-glycans on the expression of polysialic acids (PSAs), the expression of PSAs in a fucose-lacking mutant of Chinese hamster ovary (CHO) cells, Lec13, was compared with that in CHO K1 cells.
Xue-En Liu et al.
Hepatology (Baltimore, Md.), 46(5), 1426-1435 (2007-08-09)
We evaluated the use of blood serum N-glycan fingerprinting as a tool for the diagnosis of hepatocellular carcinoma (HCC) in patients with cirrhosis induced by hepatitis B virus (HBV). A group of 450 HBV-infected patients with liver fibrosis or cirrhosis
E Staudacher et al.
European journal of biochemistry, 199(3), 745-751 (1991-08-01)
Incubation of honeybee (Apis mellifica) venom-gland extracts with GDP-[14C]fucose and GlcNAc beta 1----2Man alpha 1----6(GlcNAc beta 1----2Man alpha 1----3)Man beta 1----4GlcNAc beta 1----4(Fuc alpha 1----6)GlcNAc beta 1----N-Asn-peptide(NAc) gave a labeled product in 40% yield. Analysis by 500-MHz 1H-NMR spectroscopy indicated
Naoyuki Taniguchi et al.
Current opinion in structural biology, 16(5), 561-566 (2006-09-15)
Identification of the glycosyltransferase genes that are involved in the biosynthesis of glycoconjugates has opened up new avenues in glycobiology, the decoding of the function of sugar chains. Specific biosynthesis of branched N-glycan structures by glycosyltransferases functionally modifies target glycoproteins
Studies on the Koenigs-Knorr reaction: Part II. Synthesis of an α-L-linked disaccharide from tri-O-benzyl-α-L-fucopyranosyl bromide
Dejter-Juszynski, M. and Flowers, H.M.
Carbohydrate Research, 18, 219-212 (1971)

全球贸易项目编号

货号GTIN
49095-1MG04061825659497

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