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Epostane

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Catalog No. T68664Cas No. 80471-63-2
Alias Win-32729

Epostane acts as an antiprogestogen and terminates pregnancy by inhibiting 3β-hydroxysteroid dehydrogenase and preventing the biosynthesis of progesterone and pregnenolone. [4]

Epostane

Epostane

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Catalog No. T68664Alias Win-32729Cas No. 80471-63-2
Epostane acts as an antiprogestogen and terminates pregnancy by inhibiting 3β-hydroxysteroid dehydrogenase and preventing the biosynthesis of progesterone and pregnenolone. [4]
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$623In StockIn Stock
5 mg$1,290In StockIn Stock
10 mg$1,770In StockIn Stock
25 mg$2,630In StockIn Stock
50 mg$3,550In StockIn Stock
100 mg$4,790-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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:>99.99%
Appearance:Solid
Color:White
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Product Introduction

Epostane AI Summary
Epostane shows antiviral activity against SARS-CoV-2 by inhibiting cytotoxicity in VERO-6 cells. The IC50 value for this compound is greater than 20,000 nM based on a high content imaging assay conducted after 48 hours of exposure to the virus..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Epostane acts as an antiprogestogen and terminates pregnancy by inhibiting 3β-hydroxysteroid dehydrogenase and preventing the biosynthesis of progesterone and pregnenolone. [4]
In vitro
METHODS: Using one fish oocyte, the ovary was cut into small pieces and incubated with Epostane (1 μg/mL), and the incidence of germinal vesicle breakdown (GVBD) was examined microscopically
RESULTS Epostane induced a significant decrease in the frequency of GVBD in oocytes, but Epostane failed to eliminate the maturation effect of 17α,20 β-diOHprog, the most potent maturation-inducing steroid in this species.
In vivo
METHODS: A single-dose, randomized, double-blind study was conducted in which each woman awaiting termination of pregnancy was administered either 50 mg Epostane or 100 mg Epostane orally, and the effects of in vivo serum luteinizing hormone (P), estradiol (E2), and cortisol were determined.
RESULTS Both serum P concentrations decreased significantly, and a similar decrease in serum E2 was observed, with subsequent normalization of E2. [1]
METHODS: Seventy-eight healthy women were recruited to the study who were less than 49 days from their last menstrual period and requested termination of pregnancy, 200 mg Epostane four times daily for a total of 7 days.
RESULTS The complete abortion rate in the Epostane group was 73%. [2]
SynonymsWin-32729
Chemical Properties
Molecular Weight357.49
FormulaC22H31NO3
Cas No.80471-63-2
SmilesC[C@@]12[C@]3([C@](C)(O3)C(O)=C(C#N)C1)CC[C@@]4([C@@]2(CC[C@@]5(C)[C@]4(CC[C@]5(C)O)[H])[H])[H]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.

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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:
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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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