51282
Deoxyfuconojirimycin hydrochloride
≥98.0% (TLC)
Synonym(s):
1,5-Dideoxy-1,5-imino-L-fucitol hydrochloride
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About This Item
Empirical Formula (Hill Notation):
C6H13NO3 · HCl
CAS Number:
Molecular Weight:
183.63
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
Recommended Products
Assay
≥98.0% (TLC)
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
InChI key
SHSBWMUIVLOMIL-NQZVPSPJSA-N
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.
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Cell surface associated alpha-L-fucose moieties modulate human breast cancer neoplastic progression.
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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