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Safety Information

51282

Sigma-Aldrich

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:
210174-73-5
Molecular Weight:
183.63
MDL number:
MFCD00269961
UNSPSC Code:
12352201
PubChem Substance ID:
329757678
NACRES:
NA.25

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

51282-VAR:
51282-BULK:
51282-5MG:

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Certificates of Analysis (COA)

Lot/Batch Number
BCBV0200
BCBJ1190V
BCBF8887V
BCBD2526V
BCBD2527V

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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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