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β-Nicotinamide mononucleotide, reduced form disodium

(Synonyms: NMNH disodium) Copy Product Info
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Synonyms: NMNH disodium

Catalog No. TN11626 Copy Product Info
Purity: 99.92%
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β-Nicotinamide mononucleotide, reduced form disodium is the reduced form of β-nicotinamide mononucleotide with oral bioavailability. It significantly increases cellular NAD⁺ and NADH levels, inhibits glycolysis, the tricarboxylic acid cycle, and cell growth, and its efficacy depends on nicotinamide mononucleotide adenylyltransferase (NMNAT).
β-Nicotinamide mononucleotide, reduced form disodium
Cas No. 108347-85-9
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$35-In Stock
5 mg$74-In Stock
10 mg$106-In Stock
25 mg$173-In Stock
50 mg$256-In Stock
100 mg$378-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Purity:99.92%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
β-Nicotinamide mononucleotide, reduced form disodium is the reduced form of β-nicotinamide mononucleotide with oral bioavailability. It significantly increases cellular NAD⁺ and NADH levels, inhibits glycolysis, the tricarboxylic acid cycle, and cell growth, and its efficacy depends on nicotinamide mononucleotide adenylyltransferase (NMNAT).
In vitro
Methods: HepG2 cells were treated with β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium; 100 μM was used for 12 h to detect NAD⁺ and metabolite levels, and 250–1000 μM was used for 12–72 h to detect cell growth and cell cycle.
Results:
1 β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium (100 μM, 12 h) could significantly increase the intracellular NAD⁺ level in HepG2 cells and decrease the contents of glycolysis and tricarboxylic acid cycle intermediates [1].
2 β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium (250–1000 μM, 12–72 h) could inhibit the proliferation of HepG2 cells and induce cell cycle arrest.
In vivo
Methods: Male mice were given a single administration of β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium: 340 mg/kg by intraperitoneal injection or intragastric administration, and 250 mg/kg by intraperitoneal injection, to detect NAD⁺ levels in various tissues.
Results:
1 β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium (340 mg/kg, single intraperitoneal injection / intragastric administration) could increase the liver NAD⁺ level in male mice [1].
2 β-Nicotinamide mononucleotide, reduced form disodium, reduced form (NMNH) disodium (250 mg/kg, single intraperitoneal injection) could increase the NAD⁺ levels in tissues such as liver, kidney, brain, muscle and whole blood of C57BL/6J mice by 2–5 times [2].
SynonymsNMNH disodium
Chemical Properties
Molecular Weight380.20
FormulaC11H15N2Na2O8P
Cas No.108347-85-9
SmilesO[C@H]1[C@@H](O[C@H](COP([O-])([O-])=O)[C@H]1O)N2C=C(C(N)=O)CC=C2.[Na+].[Na+]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 80 mg/mL (210.42 mM), Sonication is recommended.
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM2.6302 mL13.1510 mL26.3019 mL131.5097 mL
5 mM0.5260 mL2.6302 mL5.2604 mL26.3019 mL
10 mM0.2630 mL1.3151 mL2.6302 mL13.1510 mL
20 mM0.1315 mL0.6575 mL1.3151 mL6.5755 mL
50 mM0.0526 mL0.2630 mL0.5260 mL2.6302 mL
100 mM0.0263 mL0.1315 mL0.2630 mL1.3151 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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In Vivo Formulation Calculator (Clear solution)

Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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Related Tags: β-Nicotinamide mononucleotide, reduced form disodium chemical structure | β-Nicotinamide mononucleotide, reduced form disodium in vivo | β-Nicotinamide mononucleotide, reduced form disodium in vitro | β-Nicotinamide mononucleotide, reduced form disodium formula | β-Nicotinamide mononucleotide, reduced form disodium molecular weight