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1-Deoxynojirimycin Carbohydrate Metabolism modulator

Cat.No.S3839

1-Deoxynojirimycin (duvoglustat, moranolin) is a potent α-glucosidase inhibitor and most commonly found in mulberry leaves. It has therapeutic potency against diabetes mellitus.
1-Deoxynojirimycin Carbohydrate Metabolism modulator Chemical Structure

Chemical Structure

Molecular Weight: 163.17

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 163.17 Formula

C6H13NO4

Storage (From the date of receipt)
CAS No. 19130-96-2 Download SDF Storage of Stock Solutions

Synonyms duvoglustat, moranolin Smiles C1C(C(C(C(N1)CO)O)O)O

Solubility

In vitro
Batch:

DMSO : 33 mg/mL (202.24 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 33 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Mechanism of Action

Targets/IC50/Ki
α-glucosidase [3]
(Cell-free assay)
In vitro
1-Deoxynojirimycin (DNJ) up to 200 μmol/L does not influence survival of HUVECs. This compound behaves as an antioxidant, decreases ROS production, and delays cellular senescence[2].
In vivo
1-Deoxynojirimycin (DNJ) inhibits intestinal glucose absorption in intestine. This compound down-regulates intestinal SGLT1, Na+/K+-ATP and GLUT2 mRNA and protein expression. Pretreatment with this chemical (50 mg/kg) increases the activity, mRNA and protein levels of hepatic glycolysis enzymes (GK, PFK, PK, PDE1) and decreases the expression of gluconeogenesis enzymes (PEPCK, G-6-Pase), improves glucose tolerance in both normal and diabetic mice. It inhibits intestinal glucose absorption and accelerates hepatic glucose metabolism by directly regulating the expression of proteins involved in glucose transport systems, glycolysis and gluconeogenesis enzymes[1]. DNJ reduces oxidative stress in the liver and plasma in rodents[2].
References

Clinical Trial Information

(data from https://clinicaltrials.gov, updated on 2024-05-22)

NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT01380743 Completed
Pompe Disease
Amicus Therapeutics
October 31 2011 Phase 2

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