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Balsalazide disodium dihydrate

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Catalog No. T4615 Copy Product Info
Purity: 99.49%
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Balsalazide disodium dihydrate is an aminosalicylate prodrug that releases mesalazine (HY-15027) in the colon. It also exerts anti-inflammatory and anti-cancer effects by modulating the IL-6/STAT3 pathway, and is used in the research of inflammatory bowel disease and cancer.
Balsalazide disodium dihydrate
Cas No. 150399-21-6
Pack SizePriceUSA StockGlobal StockQuantity
5 mg$39In StockIn Stock
10 mg$59In StockIn Stock
25 mg$105In StockIn Stock
50 mg$158In StockIn Stock
100 mg$239In StockIn Stock
1 mL x 10 mM (in DMSO)$51In StockIn 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:99.49%
Appearance:Solid
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Product Introduction

Bioactivity
Description
Balsalazide disodium dihydrate is an aminosalicylate prodrug that releases mesalazine (HY-15027) in the colon. It also exerts anti-inflammatory and anti-cancer effects by modulating the IL-6/STAT3 pathway, and is used in the research of inflammatory bowel disease and cancer.
In vitro
Methods: The FLUOR DE LYS® Sirt5 Fluorometric Drug Discovery Assay Kit was used. Sirt5 enzyme was incubated with 50 μM Balsalazide disodium dihydrate for 1 hour to determine its inhibitory activity.
Results: Balsalazide disodium dihydrate inhibited 89% of Sirt5 activity at 50 μM concentration, with an IC₅₀ value of 13.8 μM. [1]
Methods: 10% rat feces, cecal, and colonic contents bioreactors were used, and drugs were anaerobically incubated at 500 μM for 240 minutes to determine degradation kinetics.
Results :The degradation rate constant of balsalazide in rat feces was 0.015 min⁻¹, which was relatively close to human data (0.009 min⁻¹). [2]
In vivo
Methods:In an AOM/DSS-induced colitis-associated colorectal cancer (CAC) mouse model, Balsalazide disodium dihydrate was administered orally by gavage at a dose of 200 mg/kg once daily (dissolved in normal saline) for three cycles.
Results: The combination treatment group showed recovery of body weight, improvement in colon shortening, and significant reduction in histological inflammation and infiltration depth scores. [3]
Chemical Properties
Molecular Weight437.31
FormulaC17H17N3Na2O8
Cas No.150399-21-6
Smiles[Na+].[Na+].O.O.O=C([O-])c1cc(ccc1O)/N=N/c2ccc(cc2)C(=O)NCCC([O-])=O
Relative Density.no data available
Storage & Solubility Information
StorageKeep away from direct sunlight Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 168.3 mg/mL (384.85 mM), Sonication is recommended.
H2O: 198.9 mM, Sonication is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.2867 mL11.4335 mL22.8671 mL114.3354 mL
5 mM0.4573 mL2.2867 mL4.5734 mL22.8671 mL
10 mM0.2287 mL1.1434 mL2.2867 mL11.4335 mL
20 mM0.1143 mL0.5717 mL1.1434 mL5.7168 mL
50 mM0.0457 mL0.2287 mL0.4573 mL2.2867 mL
100 mM0.0229 mL0.1143 mL0.2287 mL1.1434 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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Keywords

Related Tags: Balsalazide disodium dihydrate chemical structure | Balsalazide disodium dihydrate in vivo | Balsalazide disodium dihydrate in vitro | Balsalazide disodium dihydrate formula | Balsalazide disodium dihydrate molecular weight