Deoxynojirimycin Tetrabenzyl Ether
Deoxynojirimycin Tetrabenzyl Ether (CAS No.: 69567-11-9) is a synthetic derivative of the iminosugar deoxynojirimycin and is primarily utilized in biochemical and pharmacological research as a butyrylcholinesterase (BuChE) inhibitor and as a synthetic intermediate in glycosphingolipid metabolism studies. It exhibits inhibitory activity against human BuChE through interaction with the enzyme’s active site, with potency in the low micromolar range, making it a useful tool for probing cholinesterase-mediated pathways relevant to neuroendocrine regulation, drug metabolism, and neurodegenerative disorders such as Alzheimer’s disease. In addition to its cholinesterase inhibitory profile, this compound serves as a key intermediate in the preparation of glucosylceramide synthase inhibitors, linking it to pathways involved in glycosphingolipid biosynthesis and lysosomal storage disorders, and indirectly to modulation of α-glucosidase I and II through derivative compounds. As such, it is broadly applied in enzyme mechanism studies, early-stage drug discovery, and target validation assays, with experimental concentrations typically optimized according to specific cellular or biochemical assay conditions.
| Physical Appearance | A crystalline solid |
| Storage | -20°C |
| M.Wt | 523.66 |
| Cas No. | 69567-11-9 |
| Formula | C34H37NO4 |
| Synonyms | DNJ Tetrabenzyl Ether; dNM Tetrabenzyl Ether |
| Solubility | ≤0.25mg/ml in ethanol;15mg/ml in DMSO;15mg/ml in dimethyl formamide |
| Chemical Name | (2R,3R,4R,5S)-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)piperidine |
| Canonical SMILES | C1(CO[C@@H]2[C@H](NC[C@@H]([C@H]2OCC3=CC=CC=C3)OCC4=CC=CC=C4)COCC5=CC=CC=C5)=CC=CC=C1 |
| Shipping Condition | Small Molecules with Blue Ice, Modified Nucleotides with Dry Ice. |
| General tips | We do not recommend long-term storage for the solution, please use it up soon. |







