| Weight | 219.281 g/mol | 
|---|---|
| Formula | C10H21NO4 | 
| Hydrogen Acceptors | 5 | 
| Hydrogen Donors | 4 | 
| Aromatic Rings | 0 | 
| Rotatable Bonds | 4 | 
Miglustat (72599-27-0)
 Score:
          #125 in Neurology
          ,
          #567 in Neuroscience
          ,
          #2562 in Biology
          
        
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      - Sigma-Aldrich -  Miglustat100.00 - 296.00 USD
 - Fisher Scientific - Search for Miglustat
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 - Miglustat for treatment of Niemann-Pick C disease: a randomised controlled study (Lancet Neurology, 2007)
 - The role of the iminosugar N-butyldeoxynojirimycin (miglustat) in the management of type I (non-neuronopathic) Gaucher disease: A position statement (Journal of Inherited Metabolic Disease, 2003)
 - Sustained therapeutic effects of oral miglustat (Zavesca, N-butyldeoxynojirimycin, OGT 918) in type I Gaucher disease (Journal of Inherited Metabolic Disease, 2004)
 - Randomized, controlled trial of miglustat in Gaucher's disease type 3. (Annals of Neurology, 2008)
 - Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the -glucosidase inhibitor miglustat (FEBS Letters, 2006)
 - Miglustat in adult and juvenile patients with NiemannPick disease type C: Long-term data from a clinical trial (Molecular Genetics and Metabolism, 2010)
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            Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 
          SMILESCCCCN1CC(C(C(C1CO)O)O)O
 - 
          InChIKeyUQRORFVVSGFNRO-UHFFFAOYSA-N
 - Pubchem - Miglustat
 - Wikipedia - miglustat
          
          Miglustat (OGT 918, N-butyl-deoxynojirimycin) is a drug developed by Oxford GlycoSciences and marketed by Actelion and is used primarily to treat type I Gaucher disease (GD1). It is marketed under the trade name Zavesca.
 
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 Miglustat 
                  