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AZD9977

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Catalog No. T9022Cas No. 1850385-64-6
Alias AZD 9977

AZD9977 is a novel, selective modulator of mineralocorticoid receptor .

AZD9977

AZD9977

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Purity: 99.82%
Catalog No. T9022Alias AZD 9977Cas No. 1850385-64-6
AZD9977 is a novel, selective modulator of mineralocorticoid receptor .
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$34In StockIn Stock
5 mg$74In StockIn Stock
10 mg$113In StockIn Stock
25 mg$223In StockIn Stock
50 mg$337In StockIn Stock
100 mg$457In StockIn Stock
1 mL x 10 mM (in DMSO)$81In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
All TargetMol products are for research purposes only and cannot be used for human consumption. We do not provide products or services to individuals. Please comply with the intended use and do not use TargetMol products for any other purpose.
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Purity:99.82%
Appearance:Solid
Color:White
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Product Introduction

AZD9977 AI Summary
AZD9977 exhibits bioactivity through its interaction with the mineralocorticoid receptor, acting as an antagonist in both human and rat models. This interaction is demonstrated by its ability to inhibit receptor functions and affect the nuclear translocation of the receptor in human cells. In binding assays Test A1 and Test A2, the compound displayed IC50 values of 130.0 nM and 240.0 nM, respectively, indicating significant binding affinity. Furthermore, AZD9977 has notable pharmacokinetic properties, including oral bioavailability, clearance rates in rat models, and permeability in human cells..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
AZD9977 is a novel, selective modulator of mineralocorticoid receptor .
SynonymsAZD 9977
Chemical Properties
Molecular Weight399.37
FormulaC20H18FN3O5
Cas No.1850385-64-6
SmilesCNC(=O)C[C@H]1COc2cc(F)ccc2N1C(=O)c1ccc2OCC(=O)Nc2c1
Relative Density.1.377 g/cm3 (Predicted)
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: 27.5 mg/mL (68.86 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2 mg/mL (5.01 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.5039 mL12.5197 mL25.0394 mL125.1972 mL
5 mM0.5008 mL2.5039 mL5.0079 mL25.0394 mL
10 mM0.2504 mL1.2520 mL2.5039 mL12.5197 mL
20 mM0.1252 mL0.6260 mL1.2520 mL6.2599 mL
50 mM0.0501 mL0.2504 mL0.5008 mL2.5039 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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