1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE CAS 73465-43-7
Introduction:Basic information about 1-DEOXYMANNOJIRIMYCIN HYDROCHLORIDE CAS 73465-43-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
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 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. |
| InChI | 1S/C6H13NO4.ClH/c8-2-3-5(10)6(11)4(9)1-7-3;/h3-11H,1-2H2;1H/t3-,4-,5-,6-;/m1./s1 |
| InChIKey | ZJIHMALTJRDNQI-MVNLRXSJSA-N |
| SMILES | Cl.OC[C@H]1NC[C@@H](O)[C@@H](O)[C@@H]1O |
| CAS DataBase Reference | 73465-43-7 |
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 |
| Storage Class | 11 - Combustible Solids |
| Hazard Classifications | Acute Tox. 4 Dermal Acute Tox. 4 Inhalation Acute Tox. 4 Oral |
| 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 | Selective inhibitor of a-mannosidase |
| 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. |
| storage | +4°C |
| References | [1] J BISCHOFF R K L Liscum. The use of 1-deoxymannojirimycin to evaluate the role of various alpha-mannosidases in oligosaccharide processing in intact cells.[J]. The Journal of Biological Chemistry, 1986, 261 10: 4766-4774. [2] JOYCE BISCHOFF Rosalind K. The effect of 1-deoxymannojirimycin on rat liver α-mannosidases[J]. Biochemical and biophysical research communications, 1984, 125 1: Pages 324-331. DOI:10.1016/s0006-291x(84)80371-x [3] ULRIKE FUHRMANN. Novel mannosidase inhibitor blocking conversion of high mannose to complex oligosaccharides[J]. Nature, 1984, 307 5953: 755-758. DOI:10.1038/307755a0 [4] KUNIO MIYAKE Kaoru N. Inhibition of α-mannosidase attenuates endoplasmic reticulum stress-induced neuronal cell death[J]. Neurotoxicology, 2009, 30 1: Pages 144-150. DOI:10.1016/j.neuro.2008.10.010 [5] APRIL TAI. Production of lentiviral vectors with enhanced efficiency to target dendritic cells by attenuating mannosidase activity of mammalian cells.[J]. Journal of Biological Engineering, 2011, 5 1: 1. DOI:10.1186/1754-1611-5-1 [6] CHI-LIN LEE. Construction of stable producer cells to make high-titer lentiviral vectors for dendritic cell-based vaccination[J]. Biotechnology and Bioengineering, 2011, 109 6: 1551-1560. DOI:10.1002/bit.24413 |
