ChemicalBook--->CAS DataBase List--->73465-43-7

73465-43-7

73465-43-7 Structure

73465-43-7 Structure
IdentificationBack Directory
[Name]

1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE
[CAS]

73465-43-7
[Synonyms]

DMJ
DMM
DMJ, HYDROCHLORIDE
DEOXYMANNOJIRIMYCIN HCL
DEOXYMANNONOJIRIMYCIN HCL
1-DEOXYMANNOJIRIMYCIN HCL
1-DeoxymannojirimycineHCl
DEOXYMANNOJIRIMYCIN, HYDROCHLORIDE
1-Deoxymannojirimycinehydrochloride
1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE
1,5-DIDEOXY-1,5-IMINO-D-MANNITOL, HCL
Manno-1-deoxynojiriMycin Hydrochloride
(+)-1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE
1-Deoxymannojirimycin hydrochloride min. 98%
1,5-DIDEOXY-1,5-IMINO-D-MANNITOL HYDROCHLORIDE
(2R,3R,4R,5R)-2-(HYDROXYMETHYL)-3,4,5-PIPERIDINETRIOL HYDROCHLORIDE
3,4,5-Piperidinetriol, 2-(hydroxymethyl)-, hydrochloride, (2R,3R,4R,5R)-
DMJ HCl, (2R,3R,4R,5R)-2-(Hydroxymethyl)-3,4,5-piperidinetriol hydrochloride
[Molecular Formula]

C6H14ClNO4
[MDL Number]

MFCD00083611
[MOL File]

73465-43-7.mol
[Molecular Weight]

199.63
Chemical PropertiesBack Directory
[Appearance]

White Crystalline Solid
[Melting point ]

183-185°C
[storage temp. ]

2-8°C
[solubility ]

H2O: soluble10mg/mL
[form ]

Powder
[color ]

white to off-white
[Water Solubility ]

Soluble in water (50 mM)
[Stability:]

Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20°C for up to 2 months.
[CAS DataBase Reference]

73465-43-7
Hazard InformationBack Directory
[Chemical Properties]

White Crystalline Solid
[Uses]

Deoxymannojirimycin has been shown to be a potent inhibitor of the mammalian Golgi alpha- mannosidase 1 activity, blocking the conversion of high-mannose oligosaccharides to complex-type oligosaccharides. However, it does not inhibit the biosynthesis of lipid- linked oligosaccharides.
[Description]

1-Deoxymannojirimycin is a specific inhibitor of class I α-1,2-mannosidase (IC50 = 0.02 μM), a key enzyme for N-glycan processing in the endoplasmic reticulum and Golgi and for targeting misfolded proteins for translocation out of the endoplasmic reticulum and degradation by the proteasome. By inhibiting α-1,2-mannosidase activity, this compound generates N-linked oligosaccharides with high mannose content, preventing misfolded protein degradation. This compound has been used for studies on glycoprotein processing and as a model for the development of anticancer and antiviral therapies.
[storage]

+4°C
[References]

1) Bischoff et al. (1986), The use of 1-deoxymannojirimycin to evaluated the role of various alpha-mannosidases in oligosaccharide processing in intact cells; J. Biol. Chem., 261 4766 2) Bischoff et al. (1984), The effect of 1-deoxymannojirimycin on rat liver alpha mannosidases.; Biochem. Biophys. Res. Commun., 125 324 3) Fuhrmann et al. (1984), Novel mannosidase inhibitor blocking conversation of high mannose to complex oligosaccharides; Nature, 307 755 4) Miyake and Nagai (2009), Inhibition of alpha-mannosidase attenuates endoplasmic reticulum stress-induced neuronal cell death; Neurotoxicology, 30 144 5) Tai et al. (2011), Production of lentiviral vectors with enhanced efficiency to target dendritic cells by attenuating mannosidase activity of mammalian? cells; J. Biol. Eng., 5? 1 6) Lee et al. (2012), Construction of stable producer cells to make high-titer lentiviral vectors for dendritic cell-based vaccination; Biotechnol. Bioeng., 109 1551
Safety DataBack Directory
[Hazard Codes ]

Xn,Xi
[Risk Statements ]

20/21/22-36/37/38
[Safety Statements ]

22-24/25-36-37/39-26
[WGK Germany ]

3
[HS Code ]

2941900000
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