Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C6H13NO4 |
| Molecular Weight | 163.1717 |
| Optical Activity | ( + ) |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O
InChI
InChIKey=LXBIFEVIBLOUGU-JGWLITMVSA-N
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
| Molecular Formula | C6H13NO4 |
| Molecular Weight | 163.1717 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 4 / 4 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Duvoglustat, an alkaloid azasugar or iminosugar, is a biologically active natural compound that exists in mulberry leaves and Commelina communis (dayflower) as well as from several bacterial strains such as Bacillus and Streptomyces species. Duvoglustat is an investigational pharmacological chaperone for the treatment of acid α-glucosidase (GAA) deficiency, which leads to the lysosomal storage disorder Pompe disease, which is characterized by progressive accumulation of lysosomal glycogen primarily in heart and skeletal muscles. Duvoglustat possesses antihyperglycemic, anti-obesity, and antiviral features. Most importantly, pre-meal intake of duvoglustat in therapeutic concentration has resulted in the inhibition of postprandial hyperglycemia and hyperinsulinemia. Thus, duvoglustat seems to be a potential treatment for checking or setting back the inception of diabetes. No duvoglustat-related adverse events or drug-related tolerability issues were identified in phase II clinical trial for the treatment of Pompe disease.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Hypoglycemic effect of deoxynojirimycin-polysaccharide on high fat diet and streptozotocin-induced diabetic mice via regulation of hepatic glucose metabolism. | 2015-01-05 |
|
| 1-deoxynojirimycin isolated from Bacillus subtilis improves hepatic lipid metabolism and mitochondrial function in high-fat-fed mice. | 2015-01 |
|
| Inhibition of alpha-mannosidase attenuates endoplasmic reticulum stress-induced neuronal cell death. | 2009-01 |
|
| Imino sugars are potent agonists of the human glucose sensor SGLT3. | 2007-02 |
|
| Glycosylation inhibitors and neuraminidase enhance human immunodeficiency virus type 1 binding and neutralization by mannose-binding lectin. | 2003-02 |
|
| Imino sugars that are less toxic but more potent as antivirals, in vitro, compared with N-n-nonyl DNJ. | 2002-09 |
|
| N-alkylated nitrogen-in-the-ring sugars: conformational basis of inhibition of glycosidases and HIV-1 replication. | 1995-06-23 |
|
| Inhibition of alpha-glucosidase I of the glycoprotein-processing enzymes by 6-O-butanoyl castanospermine (MDL 28,574) and its consequences in human immunodeficiency virus-infected T cells. | 1994-08 |
|
| 6-0-butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs. | 1991-06 |
|
| Inhibitory effect of novel 1-deoxynojirimycin derivatives on HIV-1 replication. | 1990-10 |
|
| Attenuation of HIV-1 infectivity by an inhibitor of oligosaccharide processing. | 1990-06 |
|
| Inhibition of HIV replication by amino-sugar derivatives. | 1988-09-12 |
|
| Interference with HIV-induced syncytium formation and viral infectivity by inhibitors of trimming glucosidase. | 1987-11-05 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/28341561
Single doses - 50 mg, 100 mg, 250 mg, or 600 mg
Route of Administration:
Oral
| Substance Class |
Chemical
Created
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admin
on
Edited
Mon Mar 31 18:21:54 GMT 2025
by
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on
Mon Mar 31 18:21:54 GMT 2025
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| Record UNII |
FZ56898FLE
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| Record Status |
Validated (UNII)
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NCI_THESAURUS |
C87006
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DSLD |
1116 (Number of products:2)
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m4176
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44369
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29435
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9192
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CHEMBL307429
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1-Deoxynojirimycin
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300000034137
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DTXSID70172647
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UU-168
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FZ56898FLE
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19130-96-2
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DB03206
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C87373
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| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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TARGET -> INHIBITOR |
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ACTIVE MOIETY |
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