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Deoxycorticosterone

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Catalog No. T20302Cas No. 64-85-7
Alias Desoxycortone, Desoxycorticosteronum, Desoxycorticosterone

Deoxycorticosterone (Desoxycortone) is a steroid metabolite produced by the adrenal gland. Deoxycorticosterone is an aldosterone precursor and possesses mineralocorticoid activity.

Deoxycorticosterone

Deoxycorticosterone

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Purity: 98.19%
Catalog No. T20302Alias Desoxycortone, Desoxycorticosteronum, DesoxycorticosteroneCas No. 64-85-7
Deoxycorticosterone (Desoxycortone) is a steroid metabolite produced by the adrenal gland. Deoxycorticosterone is an aldosterone precursor and possesses mineralocorticoid activity.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$39In StockIn Stock
10 mg$64In StockIn Stock
25 mgInquiryIn StockIn Stock
50 mgInquiryIn StockIn Stock
1 mL x 10 mM (in DMSO)$45In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.19%
Appearance:Solid
Color:White
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Product Introduction

Deoxycorticosterone AI Summary
Deoxycorticosterone exhibits a range of bioactivities, prominently featuring strong binding affinities towards transport and binding proteins such as corticosteroid-binding globulin and testosterone-binding globulin, with respective Log 1/K values of 7.653 and 7.38. It has a relative binding affinity of 58.0% against the Mineralocorticoid Receptor in male Sprague-Dawley rats, reflecting a mineralocorticoid activity value of 1.0 in this model. Additionally, it demonstrates significant permeability characteristics with a division coefficient (logD7.4) of 3.08 and a skin permeability log Kp of -6.73. The compound also shows specific interactions in various cellular and enzymatic contexts, such as notable antiviral activity against SARS-CoV-2, moderate inhibition of human HDAC6 (32.24% inhibition with a commercial peptide substrate), and the potential to influence hormone-related bioactivity through displacement of sex hormones from their binding globulins and interaction with the androgen and progestin receptors. Moreover, it inhibits mouse constitutive androstane receptor activity, with 58.0% of activity remaining at 10 μM. These diverse bioactivities suggest that Deoxycorticosterone may have substantial therapeutic and pharmacological potential across multiple biological pathways and targets..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Deoxycorticosterone (Desoxycortone) is a steroid metabolite produced by the adrenal gland. Deoxycorticosterone is an aldosterone precursor and possesses mineralocorticoid activity.
Targets&IC50
Mineralocorticoid Receptor:0.16 nM (EC50)
SynonymsDesoxycortone, Desoxycorticosteronum, Desoxycorticosterone
Chemical Properties
Molecular Weight330.46
FormulaC21H30O3
Cas No.64-85-7
SmilesC[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2C(=O)CO
Relative Density.1.15 g/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: 95 mg/mL (287.48 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 3.3 mg/mL (9.99 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 mM3.0261 mL15.1304 mL30.2608 mL151.3042 mL
5 mM0.6052 mL3.0261 mL6.0522 mL30.2608 mL
10 mM0.3026 mL1.5130 mL3.0261 mL15.1304 mL
20 mM0.1513 mL0.7565 mL1.5130 mL7.5652 mL
50 mM0.0605 mL0.3026 mL0.6052 mL3.0261 mL
100 mM0.0303 mL0.1513 mL0.3026 mL1.5130 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:
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2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

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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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