1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE

1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Basic information
Product Name:1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE
Synonyms:DMJ;DMJ, HYDROCHLORIDE;DMM;DEOXYMANNOJIRIMYCIN HCL;DEOXYMANNOJIRIMYCIN, HYDROCHLORIDE;DEOXYMANNONOJIRIMYCIN HCL;1,5-DIDEOXY-1,5-IMINO-D-MANNITOL, HCL;1,5-DIDEOXY-1,5-IMINO-D-MANNITOL HYDROCHLORIDE
CAS:73465-43-7
MF:C6H14ClNO4
MW:199.63
EINECS:
Product Categories:Miscellaneous Natural Products;All Inhibitors;Glycosidase Inhibitors;Inhibitors
Mol File:73465-43-7.mol
1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Structure
1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Chemical Properties
Melting point 183-185°C
storage temp. Inert atmosphere,Store in freezer, under -20°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 Reference73465-43-7
Safety Information
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
MSDS Information
1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Usage And Synthesis
Description1-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.
Chemical PropertiesWhite Crystalline Solid
UsesDeoxymannojirimycin 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.
UsesSelective inhibitor of a-mannosidase
storage+4°C
References1) 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
1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Preparation Products And Raw materials
Clindamycin hydrochloride SWAINSONINE Mannan Oligosaccharides GF109203X A 967079 Bleomycin A5 SKF 96365 HYDROCHLORIDE terramycin hy drochloride,oxytetracycline hydrochl Doxycycline 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE 3-Hydroxypiperidine hydrochloride 2-CHLORO-2-DEOXY-ALPHA-D-GLUCOPYRANOSYL(1-3)-1-DEOXY-MANNOJIRIMYCIN DEOXYMANNOJIRIMYCIN N-ButyldeoxymannojirimycinHCl (R)-3-ISOPROPYLAMINO-1,2-PROPANEDIOL (R)-3-Hydroxypiperidine hydrocloride

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