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260575

Sigma-Aldrich

1-Deoxymannojirimycin, Hydrochloride

A specific α-mannosidase I inhibitor that blocks conversion of high mannose to complex oligosaccharides.

Sinónimos:

1-Deoxymannojirimycin, Hydrochloride, DMJ, 1,5-Dideoxy-1,5-imino-D-mannitol, HCl

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About This Item

Fórmula empírica (notación de Hill):
C6H13NO4 · xHCl
Número de CAS:
Peso molecular:
163.17 (free base basis)
UNSPSC Code:
12352200

Quality Level

assay

≥98% (TLC)

form

crystalline solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze
desiccated (hygroscopic)

color

white

solubility

ethanol: 1 mg/mL
water: 1 mg/mL

shipped in

ambient

storage temp.

−20°C

InChI

1S/C6H13NO4/c8-2-3-5(10)6(11)4(9)1-7-3/h3-11H,1-2H2/t3-,4-,5-,6-/m1/s1

InChI key

LXBIFEVIBLOUGU-KVTDHHQDSA-N

General description

A specific α-mannosidase I inhibitor that blocks conversion of high mannose to complex oligosaccharides.
Special α-mannosidase I inhibitor that blocks conversion of high mannose to complex oligosaccharides.

Biochem/physiol Actions

Cell permeable: no
Primary Target
α-mannosidase-I
Product does not compete with ATP.
Reversible: no

Packaging

Packaged under inert gas

Warning

Toxicity: Harmful (C)

Reconstitution

Following reconstitution, aliquot and freeze (-20°C) for long term storage or refrigerate (4°C) for short term storage. Stock solutions are stable for up to 1 month at 4°C or for up to 6 months at -20°C.

Other Notes

Suzuki, S.S., and Piette, L.H. 1993. J. Cell. Biochem.51, 181.
Fuhrmann, U., et al. 1984. Nature307, 755.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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U Fuhrmann et al.
Nature, 307(5953), 755-758 (1984-02-23)
Many secretory and membrane proteins are glycoproteins carrying asparagine-linked (N-linked) oligosaccharides. There are two types of N-linked glycans, referred to as high-mannose and complex type, respectively. Biosynthesis of N-linked glycans of the complex type proceeds via a high-mannose intermediate. After
S S Suzuki et al.
Journal of cellular biochemistry, 51(2), 181-189 (1993-02-01)
The mouse embryo fibroblast cell line, C3H/10T1/2, synthesized and deposited a large amount of fibronectin especially in the pericellular matrix. Confluent cultures of these cells cultured in the presence of 0.3 micrograms/ml of retinyl acetate released cell surface fibronectin and

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