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1-DEOXYNOJIRIMYCIN
SpectraBase Compound ID Fd7WV9cH1kp
InChI InChI=1S/C6H13NO4/c8-2-3-5(10)6(11)4(9)1-7-3/h3-11H,1-2H2/t3-,4+,5-,6-/m1/s1
InChIKey LXBIFEVIBLOUGU-JGWLITMVSA-N
Mol Weight 163.17 g/mol
Molecular Formula C6H13NO4
Exact Mass 163.084458 g/mol
Enantiomer InChIKey LXBIFEVIBLOUGU-FSIIMWSLSA-N
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum O-19-177-1
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum J-52-3341-2
Copyright Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum E1-37-3704-1
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent D2O
  • MORANOLINE;1-DEOXY-NOJIRIMYCIN
  • SGI;1-DEOXYNOJIRIMYCIN
  • 1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
  • (2R,3R,4R,5S)-2-(hydroxymethyl)-3,4,5-piperidinetriol
Title Journal or Book Year
Nitrogen-Containing Furanose and Pyranose Analogues from Hyacinthus orientalis Journal of Natural Products 1998
Use of (chloromethyl) dimethylphenylsilane in sugar chemistry. Stereo-controlled approach to destomic acid and 1-deoxy-nojirimycin Recueil des Travaux Chimiques des Pays-Bas 1993
Isolation and characterization of amylase inhibitors, (glucose)ndeoxynojirimycin. Agricultural and Biological Chemistry 1986
Enzymatic synthesis of 4-O-.ALPHA.-D-glucopyranosyl-moranoline. Agricultural and Biological Chemistry 1985

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