1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE manufacturers
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| 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Basic information |
Product Name: | 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE | Synonyms: | 1,5-DIDEOXY-1,5-IMINO-D-MANNITOL, HCL;1,5-DIDEOXY-1,5-IMINO-D-MANNITOL HYDROCHLORIDE;1-DEOXYMANNOJIRIMYCIN HCL;(+)-1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE;1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE;(2R,3R,4R,5R)-2-(HYDROXYMETHYL)-3,4,5-PIPERIDINETRIOL HYDROCHLORIDE;1-DeoxymannojirimycineHCl;1-Deoxymannojirimycinehydrochloride | 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 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 Reference | 73465-43-7 |
| 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Usage And Synthesis |
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. | 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. | Uses | Selective inhibitor of a-mannosidase | 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 |
| 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE Preparation Products And Raw materials |
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