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15-keto-Prostaglandin E2

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Catalog No. T78582Cas No. 26441-05-4
Alias 15-keto-PGE2

15-keto-Prostaglandin E2 is an endogenous bioactive metabolite that inhibits STAT3 activation through covalent interaction with the Cys259 residue, while also binding to and stabilizing EP2 and EP4 receptors, thereby exerting inhibitory effects on breast cancer cell growth and tumor progression, activating PPAR-γ signaling, and promoting fungal growth, collectively positioning this lipid mediator as a multifunctional regulator in cancer biology, immunometabolism, and host–pathogen interaction research.

15-keto-Prostaglandin E2

15-keto-Prostaglandin E2

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Purity: 98.31%
Catalog No. T78582Alias 15-keto-PGE2Cas No. 26441-05-4
15-keto-Prostaglandin E2 is an endogenous bioactive metabolite that inhibits STAT3 activation through covalent interaction with the Cys259 residue, while also binding to and stabilizing EP2 and EP4 receptors, thereby exerting inhibitory effects on breast cancer cell growth and tumor progression, activating PPAR-γ signaling, and promoting fungal growth, collectively positioning this lipid mediator as a multifunctional regulator in cancer biology, immunometabolism, and host–pathogen interaction research.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 μg$123-In Stock
1 mg$218-In Stock
5 mg$543-In Stock
10 mg$773-In Stock
25 mg$1,160-In Stock
50 mg$1,560-In Stock
100 mg$2,090-In 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:98.31%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
15-keto-Prostaglandin E2 is an endogenous bioactive metabolite that inhibits STAT3 activation through covalent interaction with the Cys259 residue, while also binding to and stabilizing EP2 and EP4 receptors, thereby exerting inhibitory effects on breast cancer cell growth and tumor progression, activating PPAR-γ signaling, and promoting fungal growth, collectively positioning this lipid mediator as a multifunctional regulator in cancer biology, immunometabolism, and host–pathogen interaction research.
In vivo
In a mouse xenograft model using MDA-MB-231 cells, intraperitoneal (i.p.) injection of 15-keto-Prostaglandin E2 suppressed tumor growth, resulting in reduced tumor volume and weight. This reduction correlates with the downregulation of p-STAT3 and Cyclin D1 levels in the tumor tissues [1].
Synonyms15-keto-PGE2
Chemical Properties
Molecular Weight350.45
FormulaC20H30O5
Cas No.26441-05-4
SmilesC(/C=C\CCCC(O)=O)[C@@H]1[C@@H](/C=C/C(CCCCC)=O)[C@H](O)CC1=O
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (228.28 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.8535 mL14.2674 mL28.5347 mL142.6737 mL
5 mM0.5707 mL2.8535 mL5.7069 mL28.5347 mL
10 mM0.2853 mL1.4267 mL2.8535 mL14.2674 mL
20 mM0.1427 mL0.7134 mL1.4267 mL7.1337 mL
50 mM0.0571 mL0.2853 mL0.5707 mL2.8535 mL
100 mM0.0285 mL0.1427 mL0.2853 mL1.4267 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:
% DMSO
%
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