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Risedronate Sodium

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Catalog No. T1041Cas No. 115436-72-1
Alias Risedronic Acid Sodium, NE 58095 Sodium

Risedronate Sodium (NE 58095 Sodium) is an aminobisphosphonate derivative of etidronic acid and CALCIUM CHANNEL BLOCKER that inhibits BONE RESORPTION and is used for the treatment of OSTEOPOROSIS.

Risedronate Sodium

Risedronate Sodium

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Purity: 99.72%
Catalog No. T1041Alias Risedronic Acid Sodium, NE 58095 SodiumCas No. 115436-72-1
Risedronate Sodium (NE 58095 Sodium) is an aminobisphosphonate derivative of etidronic acid and CALCIUM CHANNEL BLOCKER that inhibits BONE RESORPTION and is used for the treatment of OSTEOPOROSIS.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
50 mg$30In StockIn Stock
100 mg$40In StockIn Stock
500 mg$73In StockIn Stock
1 g$98-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.72%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Risedronate Sodium (NE 58095 Sodium) is an aminobisphosphonate derivative of etidronic acid and CALCIUM CHANNEL BLOCKER that inhibits BONE RESORPTION and is used for the treatment of OSTEOPOROSIS.
In vitro
Risedronate prevents the reduction of periosteal formation and the increase of endocortical bone resorption, thereby preserving the percentage of cortical bone and marrow area. It enhances osteoblast density and lacunar occupancy while preventing the augmentation of cortical bone porosity induced by GCs. Risedronate and Vitamin K(2) exhibit additive effects on bone density and lacunar occupancy and synergistic action against cortical bone porosity. At a dosage of 1 mg/kg in rats, Risedronate significantly increases the volumetric density of bone (Vb) and osteoblasts (Vob) and more notably reduces Vm. In rats, Risedronate dose-dependently and significantly decreases tooth movement following orthodontic force application.
In vivo
At a concentration of 1 μM, Risedronate reduced the formation of colonies exhibiting osteoblastic characteristics, such as collagen accumulation, alkaline phosphatase expression, and mineralization. Conversely, 1 nM Risedronate and sodium alendronate increased the formation of fibroblast colonies, while not affecting the formation of colonies with osteoblastic traits. Risedronate completely inhibited the formation of fibroblastic colony-forming units in the calcification culture of rat bone marrow cells, whereas etidronate sodium had a comparatively lower effect. Additionally, Risedronate significantly suppressed the expression of c-Fos and nuclear factors in bone marrow-derived macrophages, specifically inhibiting the RANKL-induced activation of T cell clone c1.
SynonymsRisedronic Acid Sodium, NE 58095 Sodium
Chemical Properties
Molecular Weight305.09
FormulaC7H10NNaO7P2
Cas No.115436-72-1
Smiles[Na+].OC(Cc1cccnc1)(P(O)(O)=O)P(O)([O-])=O
Relative Density.no data available
Storage & Solubility Information
StorageIn solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
H2O: 10 mM, Sonication is recommended.
DMSO: Insoluble
Solution Preparation Table
H2O
1mg5mg10mg50mg
1 mM3.2777 mL16.3886 mL32.7772 mL163.8861 mL
5 mM0.6555 mL3.2777 mL6.5554 mL32.7772 mL
10 mM0.3278 mL1.6389 mL3.2777 mL16.3886 mL

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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:
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2 Enter the in vivo formulation:
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