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Emodinanthrone

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Catalog No. TN6740Cas No. 491-60-1
Alias emodinol, Emodin anthrone, Emodin anthranol

Emodinanthrone is a natural product belongs to the class of organic compounds known as anthracenes.

Emodinanthrone

Emodinanthrone

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Purity: 99.1%
Catalog No. TN6740Alias emodinol, Emodin anthrone, Emodin anthranolCas No. 491-60-1
Emodinanthrone is a natural product belongs to the class of organic compounds known as anthracenes.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$30In StockIn Stock
5 mg$44In StockIn Stock
10 mg$61In StockIn Stock
25 mg$98In StockIn Stock
50 mg$143In StockIn Stock
100 mg$209In StockIn Stock
200 mg$312-In Stock
1 mL x 10 mM (in DMSO)$48In 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:99.1%
Appearance:Solid
Color:Yellow
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Product Introduction

Emodinanthrone AI Summary
Emodinanthrone exhibits moderate lipophilicity with a LogP value of 3.9 and demonstrates significant antioxidant potential, evidenced by a reducing activity against 2,2-diphenyl-1-picrylhydrazyl (kDPPH = 21.4 M-1 s-1). It also shows peroxidant properties, characterized by a release ratio of 2.04 uMol of malondialdehyde to mMol of deoxyribose. The compound acts as a 5-LO inhibitor with an IC50 value of 14000.0 nM and has antiproliferative effects on HaCaT cells, with an IC50 greater than 5000.0 nM. Cytotoxicity is observed at a concentration of 2 uM, resulting in the release of 114.0 mU of LDH in HaCaT cells. Furthermore, Emodinanthrone demonstrates cytotoxic effects against human KB cells with an IC50 of 3900.0 nM. It shows weak displacement activity on the human platelet P2Y12 receptor with a Ki greater than 10000 nM and has negligible inhibition, with an inhibition rate of only 1.0% at 10 uM. Additionally, it does not inhibit ATP citrate lyase activity at 10 uM, as determined by the ADP-Glo luminescence assay..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Emodinanthrone is a natural product belongs to the class of organic compounds known as anthracenes.
Synonymsemodinol, Emodin anthrone, Emodin anthranol
Chemical Properties
Molecular Weight256.25
FormulaC15H12O4
Cas No.491-60-1
SmilesO=C1C=2C(CC=3C1=C(O)C=C(O)C3)=CC(C)=CC2O
Relative Density.1.471 g/cm3
Storage & Solubility Information
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 55 mg/mL (214.63 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.9024 mL19.5122 mL39.0244 mL195.1220 mL
5 mM0.7805 mL3.9024 mL7.8049 mL39.0244 mL
10 mM0.3902 mL1.9512 mL3.9024 mL19.5122 mL
20 mM0.1951 mL0.9756 mL1.9512 mL9.7561 mL
50 mM0.0780 mL0.3902 mL0.7805 mL3.9024 mL
100 mM0.0390 mL0.1951 mL0.3902 mL1.9512 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

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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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