Duvoglustat (1-Deoxynojirimycin)

Alias: BAY-h5595 DuvoglustatBAY-h-5595 1-deoxynojirimycinBAY-h 5595
Cat No.:V32050 Purity: ≥98%
Duvoglustat (Moranoline; deoxynojirimycin;1-Deoxynojirimycin;AT-2220; DNJ) is a novel and potent alpha-glucosidase inhibitorfound in mulberry leaves and hasantihyperglycemic, anti-obesity, and antiviral activities.
Duvoglustat (1-Deoxynojirimycin) Chemical Structure CAS No.: 19130-96-2
Product category: Glucosidase
This product is for research use only, not for human use. We do not sell to patients.
Size Price Stock Qty
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Other Forms of Duvoglustat (1-Deoxynojirimycin):

  • Duvoglustat hydrochloride
Official Supplier of:
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Top Publications Citing lnvivochem Products
Product Description

Description: Duvoglustat (Moranoline; deoxynojirimycin; 1-Deoxynojirimycin; AT-2220; DNJ) is a novel and potent alpha-glucosidase inhibitor found in mulberry leaves and has antihyperglycemic, anti-obesity, and antiviral activities. Duvoglustat can suppress the elevation of postprandial hyperglycemia, thus acting as an antihyperglycemic agent by slowing the rate of carbohydrate degradation to monosaccharides. 1-Deoxynojirimycin is most commonly found in mulberry leaves. Although it can be obtained in small quantities by brewing an herbal tea from mulberry leaves, interest in commercial production has led to research on developing mulberry tea higher in DNJ, and on alternate routes of production, such as via Bacillusspecies.

Biological Activity I Assay Protocols (From Reference)
ln Vivo
1-Deoxynojirimycin (Duvoglustat) (20 -80 mg/kg; iv; once daily for 4 weeks) has consequences that are antiphysiological [3]. 1-Deoxynojirimycin enhances insulin symptoms noticeably by triggering the db/db shark shark pattern.
Animal Protocol
Animal/Disease Models: db/db mice[3]
Doses: 20, 40, 80 mg/kg
Route of Administration: intravenous (iv) (iv)injection; signal load PI3K/AKT[ 3]. one time/day for four weeks
Experimental Results: Significant reduction in body weight, blood glucose, and serum insulin levels; improved glucose tolerance and insulin tolerance.
References
[1]. Gao K, et al. 1-Deoxynojirimycin: Occurrence, Extraction, Chemistry, Oral Pharmacokinetics, Biological Activities and In Silico Target Fishing. Molecules. 2016 Nov 23;21(11). pii: E1600.
[2]. Chaluntorn Vichasilp,et al. Development of high 1-deoxynojirimycin (DNJ) content mulberry tea and use of response surface methodology to optimize tea-making conditions for highest DNJ extraction. LWT - Food Science and Technology. Volume 45, Issue 2, March 2012, Pages 226-232
[3]. Liu Q, et al. 1-Deoxynojirimycin Alleviates Insulin Resistance via Activation of Insulin Signaling PI3K/AKT Pathway in Skeletal Muscle of db/db Mice. Molecules. 2015 Dec 4;20(12):21700-14.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C₆H₁₃NO₄
Molecular Weight
163.17
CAS #
19130-96-2
Related CAS #
1-Deoxynojirimycin hydrochloride;73285-50-4
SMILES
O[C@@H]1[C@@H](CO)NC[C@H](O)[C@H]1O
InChi Key
LXBIFEVIBLOUGU-JGWLITMVSA-N
InChi Code
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
Chemical Name
(2R,3R,4R,5S)-2-(Hydroxymethyl)piperidine-3,4,5-triol
Synonyms
BAY-h5595 DuvoglustatBAY-h-5595 1-deoxynojirimycinBAY-h 5595
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
H2O : ≥ 34 mg/mL (~208.37 mM)
Solubility (In Vivo)
Solubility in Formulation 1: 100 mg/mL (612.86 mM) in PBS (add these co-solvents sequentially from left to right, and one by one), clear solution; with sonication.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 6.1286 mL 30.6429 mL 61.2858 mL
5 mM 1.2257 mL 6.1286 mL 12.2572 mL
10 mM 0.6129 mL 3.0643 mL 6.1286 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

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Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
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Method for preparing DMSO stock solution mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

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

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
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