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 |
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Inhibition of HIV replication by amino-sugar derivatives. | 1988 Sep 12 |
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Attenuation of HIV-1 infectivity by an inhibitor of oligosaccharide processing. | 1990 Jun |
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Inhibitory effect of novel 1-deoxynojirimycin derivatives on HIV-1 replication. | 1990 Oct |
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6-0-butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs. | 1991 Jun |
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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 Aug |
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N-alkylated nitrogen-in-the-ring sugars: conformational basis of inhibition of glycosidases and HIV-1 replication. | 1995 Jun 23 |
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Imino sugars are potent agonists of the human glucose sensor SGLT3. | 2007 Feb |
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Inhibition of alpha-mannosidase attenuates endoplasmic reticulum stress-induced neuronal cell death. | 2009 Jan |
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1-deoxynojirimycin isolated from Bacillus subtilis improves hepatic lipid metabolism and mitochondrial function in high-fat-fed mice. | 2015 Jan |
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
by
admin
on
Edited
Fri Dec 15 16:12:36 GMT 2023
by
admin
on
Fri Dec 15 16:12:36 GMT 2023
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Record UNII |
FZ56898FLE
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Record Status |
Validated (UNII)
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Record Version |
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C87006
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DSLD |
1116 (Number of products:2)
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Code System | Code | Type | Description | ||
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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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Related Record | Type | Details | ||
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ACTIVE MOIETY |
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