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Merck
CN

51282

Deoxyfuconojirimycin 盐酸盐

≥98.0% (TLC)

别名:

1,5-Dideoxy-1,5-imino-L-fucitol 盐酸盐

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经验公式(希尔记法):
C6H13NO3 · HCl
化学文摘社编号:
分子量:
183.63
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352201
MDL number:
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InChI key

SHSBWMUIVLOMIL-NQZVPSPJSA-N

SMILES string

Cl.C[C@@H]1NC[C@@H](O)[C@H](O)[C@@H]1O

InChI

1S/C6H13NO3.ClH/c1-3-5(9)6(10)4(8)2-7-3;/h3-10H,2H2,1H3;1H/t3-,4+,5+,6-;/m0./s1

assay

≥98.0% (TLC)

Biochem/physiol Actions

Deoxyfuconojirimycin is a specific and competitive inhibitor of human liver α-L-fucosidase.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

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

存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Kun Yuan et al.
Pathology oncology research : POR, 14(2), 145-156 (2008-06-17)
Glycosylation drives critical processes important for mammalian cell-cell and cell-matrix interactions. Alpha-L-fucose (alpha-L-f) is a key monosaccharide component of oligosaccharides that has been found to be overexpressed during tumor progression. Modification of cell surface fucosylation, we hypothesized, alters tumor cell

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