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Details

Stereochemistry ABSOLUTE
Molecular Formula C6H13NO4.ClH
Molecular Weight 199.633
Optical Activity ( + )
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DUVOGLUSTAT HYDROCHLORIDE

SMILES

Cl.OC[C@H]1NC[C@H](O)[C@@H](O)[C@@H]1O

InChI

InChIKey=ZJIHMALTJRDNQI-VFQQELCFSA-N
InChI=1S/C6H13NO4.ClH/c8-2-3-5(10)6(11)4(9)1-7-3;/h3-11H,1-2H2;1H/t3-,4+,5-,6-;/m1./s1

HIDE SMILES / InChI
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

PubMed

TitleDatePubMed
Interference with HIV-induced syncytium formation and viral infectivity by inhibitors of trimming glucosidase.
1987 Nov 5-11
Inhibition of HIV replication by amino-sugar derivatives.
1988 Sep 12
Attenuation of HIV-1 infectivity by an inhibitor of oligosaccharide processing.
1990 Jun
Inhibitory effect of novel 1-deoxynojirimycin derivatives on HIV-1 replication.
1990 Oct
6-0-butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs.
1991 Jun
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
N-alkylated nitrogen-in-the-ring sugars: conformational basis of inhibition of glycosidases and HIV-1 replication.
1995 Jun 23
Imino sugars that are less toxic but more potent as antivirals, in vitro, compared with N-n-nonyl DNJ.
2002 Sep
Glycosylation inhibitors and neuraminidase enhance human immunodeficiency virus type 1 binding and neutralization by mannose-binding lectin.
2003 Feb
Imino sugars are potent agonists of the human glucose sensor SGLT3.
2007 Feb
Inhibition of alpha-mannosidase attenuates endoplasmic reticulum stress-induced neuronal cell death.
2009 Jan
1-deoxynojirimycin isolated from Bacillus subtilis improves hepatic lipid metabolism and mitochondrial function in high-fat-fed mice.
2015 Jan
Hypoglycemic effect of deoxynojirimycin-polysaccharide on high fat diet and streptozotocin-induced diabetic mice via regulation of hepatic glucose metabolism.
2015 Jan 5
Patents

Sample Use Guides

Single doses - 50 mg, 100 mg, 250 mg, or 600 mg
Route of Administration: Oral
Name Type Language
DUVOGLUSTAT HYDROCHLORIDE
USAN  
USAN  
Official Name English
MORANOLINE HYDROCHLORIDE
Common Name English
(+)-1-DEOXYNOJIRIMYCIN HYDROCHLORIDE
Common Name English
1 DEOXYNOJIRIMYCIN HYDROCHLORIDE
Common Name English
(2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-triol hydrochloride
Systematic Name English
AT-2220
Code English
DUVOGLUSTAT HCL
Common Name English
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, HYDROCHLORIDE, (2R-(2.ALPHA.,3.BETA.,4.ALPHA.,5.BETA.))-
Common Name English
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, HYDROCHLORIDE (1:1), (2R,3R,4R,5S)-
Common Name English
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, HYDROCHLORIDE, (2R,3R,4R,5S)-
Systematic Name English
AT2220
Code English
DUVOGLUSTAT HYDROCHLORIDE [USAN]
Common Name English
1-DEOXYNOJIRIMYCIN HYDROCHLORIDE
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 238507
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
NCI_THESAURUS C87006
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
Code System Code Type Description
PUBCHEM
13018787
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
PRIMARY
ChEMBL
CHEMBL307429
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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DRUG BANK
DB05200
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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CAS
73285-50-4
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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NCI_THESAURUS
C87374
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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SMS_ID
300000041403
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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EPA CompTox
DTXSID401017351
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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USAN
UU-169
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
PRIMARY
FDA UNII
0RN23C42QR
Created by admin on Fri Dec 15 17:41:57 GMT 2023 , Edited by admin on Fri Dec 15 17:41:57 GMT 2023
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