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(S)-Mapracorat

🥰Excellent
Catalog No. T13451Cas No. 887375-15-7
Alias (S)-ZK-245186, (S)-BOL-303242X

(S)-Mapracorat is a selective and less active agonist of the glucocorticoid receptor.

(S)-Mapracorat

(S)-Mapracorat

🥰Excellent
Catalog No. T13451Alias (S)-ZK-245186, (S)-BOL-303242XCas No. 887375-15-7
(S)-Mapracorat is a selective and less active agonist of the glucocorticoid receptor.
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Product Introduction

Bioactivity
Description
(S)-Mapracorat is a selective and less active agonist of the glucocorticoid receptor.
In vivo
During the 60-minute observation period, intradermal injection of compound 48/80 (50 μg in 50 μL saline) resulted in a significant wheal and flare reaction. Topical pre-treatment with (S)-Mapracorat (0.1%) leads to significant reduction in the wheal and flare responses compared to vehicle (acetone) treated areas.
Synonyms(S)-ZK-245186, (S)-BOL-303242X
Chemical Properties
Molecular Weight462.48
FormulaC25H26F4N2O2
Cas No.887375-15-7
SmilesCc1ccc2c(NC[C@@](O)(CC(C)(C)c3cc(F)cc4CCOc34)C(F)(F)F)cccc2n1
Relative Density.1.31g/cm3
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
DMSO: 50.6 mg/mL (109.41 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1623 mL10.8113 mL21.6226 mL108.1128 mL
5 mM0.4325 mL2.1623 mL4.3245 mL21.6226 mL
10 mM0.2162 mL1.0811 mL2.1623 mL10.8113 mL
20 mM0.1081 mL0.5406 mL1.0811 mL5.4056 mL
50 mM0.0432 mL0.2162 mL0.4325 mL2.1623 mL
100 mM0.0216 mL0.1081 mL0.2162 mL1.0811 mL

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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

You can also refer to dose conversion for different animals. More Dose Conversion

Tech Support

Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc

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