For research use only. Not for therapeutic Use.
N-Butyldeoxynojirimycin Hydrochloride-d9(Cat No.:C000554)is a deuterated analog of N-butyldeoxynojirimycin, a compound used primarily in biochemical research. The deuterium isotope substitution (denoted by “-d9”) in the molecule replaces hydrogen atoms with deuterium, enabling its use in isotope-labeled studies, such as tracking metabolic pathways and enzymatic processes. N-butyldeoxynojirimycin is an iminosugar known for inhibiting glycosidases, particularly in studies related to carbohydrate metabolism and viral infections like HIV. The deuterated version, N-Butyldeoxynojirimycin Hydrochloride-d9, is utilized in research to provide more precise data without affecting the compound’s biological activity.
Catalog Number | C000554 |
CAS Number | 1883545-57-0 |
Synonyms | (2R,3R,4R,5S)-1-Butyl-2-(hydroxymethyl)-,3,4,5-Piperidinetriol Hydrochloride-d9; Miglustat Hydrochloride-d9; |
Molecular Formula | C₁₀H₁₃D₉ClNO₄ |
Purity | ≥95% |
Solubility | Methanol (Slightly, Sonicated), Water (Slightly) |
Appearance | White to Off-White Solid |
Storage | 4°C |
IUPAC Name | (2R,3R,4R,5S)-2-(hydroxymethyl)-1-(1,1,2,2,3,3,4,4,4-nonadeuteriobutyl)piperidine-3,4,5-triol;hydrochloride |
InChI | InChI=1S/C10H21NO4.ClH/c1-2-3-4-11-5-8(13)10(15)9(14)7(11)6-12;/h7-10,12-15H,2-6H2,1H3;1H/t7-,8+,9-,10-;/m1./s1/i1D3,2D2,3D2,4D2; |
InChIKey | QPAFAUYWVZMWPR-LQJTUGORSA-N |
SMILES | [2H]C([2H])([2H])C([2H])([2H])C([2H])([2H])C([2H])([2H])N1C[C@@H]([C@H]([C@@H]([C@H]1CO)O)O)O.Cl |
Reference | Hettkamp, H., et al.: Eur. J. Biochem., 142, 85 (1984), Szumilo, T., et al.: Arch. Biochem. Biophys., 247, 261 (1986), Fleet, G.W.J., et al.: FEBS Letters, 237, Number 1,2, 128 (1988), Kolter, T., et al.: Angew. Chem. Int. Ed. Engl., 36, 1955 (1997), |