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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
Structure of DUVOGLUSTAT

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

HIDE SMILES / InChI

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

PubMed

TitleDatePubMed
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 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
Patents

Sample Use Guides

Single doses - 50 mg, 100 mg, 250 mg, or 600 mg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:12:36 GMT 2023
Edited
by admin
on Fri Dec 15 16:12:36 GMT 2023
Record UNII
FZ56898FLE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DUVOGLUSTAT
INN   USAN  
INN   USAN  
Official Name English
1,5-DIDEOXY-1,5-IMINO-D-GLUCITOL
Common Name English
5-AMINO-1,5-DIDEOXY-D-GLUCOPYRANOSE
Common Name English
BAY-H-5595
Code English
duvoglustat [INN]
Common Name English
(2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-triol
Systematic Name English
DEOXYNOJIRIMYCIN
Common Name English
MORANOLINE
Common Name English
D-1-DEOXYNOJIRIMYCIN
Common Name English
MORANOLIN
Common Name English
NOJIRIMYCIN, 1-DEOXY-
Common Name English
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, (2R,3R,4R,5S)-
Systematic Name English
3,4,5-PIPERIDINETRIOL, 2-(HYDROXYMETHYL)-, (2R-(2.ALPHA.,3.BETA.,4.ALPHA.,5.BETA.))-
Common Name English
1,5-DIDEOXY-1,5-IMINO-
Common Name English
GLUCOPYRANOSE, 5-AMINO-1,5-DIDEOXY-, D-
Common Name English
1-DEOXYNOJIRIMYCIN [MI]
Common Name English
1 DEOXYNOJIRIMYCIN
Common Name English
DUVOGLUSTAT [USAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C87006
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
DSLD 1116 (Number of products:2)
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
Code System Code Type Description
MERCK INDEX
m4176
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY Merck Index
CHEBI
44369
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
PUBCHEM
29435
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
INN
9192
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
ChEMBL
CHEMBL307429
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
WIKIPEDIA
1-Deoxynojirimycin
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
SMS_ID
300000034137
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
EPA CompTox
DTXSID70172647
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
USAN
UU-168
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
FDA UNII
FZ56898FLE
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
CAS
19130-96-2
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
DRUG BANK
DB03206
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
NCI_THESAURUS
C87373
Created by admin on Fri Dec 15 16:12:36 GMT 2023 , Edited by admin on Fri Dec 15 16:12:36 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY