Miglustat
| Clinical data | |
|---|---|
| Trade names | Zavesca, Brazaves, Opfolda | 
| Other names | OGT 918, 1,5-(butylimino)-1,5-dideoxy-D-glucitol, N-butyl-deoxynojirimycin (NB-DNJ) | 
| AHFS/Drugs.com | Monograph | 
| MedlinePlus | a604015 | 
| License data | |
| Pregnancy category | 
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| Routes of administration | By mouth | 
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Bioavailability | 97% | 
| Protein binding | Nil | 
| Metabolism | Nil | 
| Elimination half-life | 6–7 hours | 
| Excretion | Kidney, unchanged | 
| Identifiers | |
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| CAS Number | |
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| ChemSpider | |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.216.074 | 
| Chemical and physical data | |
| Formula | C10H21NO4 | 
| Molar mass | 219.281 g·mol−1 | 
| 3D model (JSmol) | |
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Miglustat, sold under the brand name Zavesca among others, is a medication used to treat type I Gaucher disease and Pompe disease.
It was approved for medical use in the European Union in November 2002, and for medical use in the United States in July 2003.