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Atractylenolide III

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Catalog No. T3902Cas No. 73030-71-4
Alias ICodonolactone, 8β-Hydroxyasterolide

Atractylenolide III (ICodonolactone) may have therapeutic potential in treating homocysteine-mediated cognitive impairment and neuronal injury. Atractylenolide III is a potential candidate for the treatment of human lung carcinoma by inducing the release of cytochrome c, upregulating the expression of Bax and translocating apoptosis-inducing factor.

Atractylenolide III

Atractylenolide III

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🥰Excellent
Purity: 99.98%
Catalog No. T3902Alias ICodonolactone, 8β-HydroxyasterolideCas No. 73030-71-4
Atractylenolide III (ICodonolactone) may have therapeutic potential in treating homocysteine-mediated cognitive impairment and neuronal injury. Atractylenolide III is a potential candidate for the treatment of human lung carcinoma by inducing the release of cytochrome c, upregulating the expression of Bax and translocating apoptosis-inducing factor.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
2 mg$33In StockIn Stock
5 mg$51In StockIn Stock
10 mg$79In StockIn Stock
25 mg$129In StockIn Stock
50 mg$189In StockIn Stock
100 mg$283In StockIn Stock
200 mg$419In StockIn Stock
1 mL x 10 mM (in DMSO)$56In 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:99.98%
Color:White to Yellow
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Product Introduction

Atractylenolide III AI Summary
Atractylenolide III exhibits multiple bioactivities across various biological systems. It demonstrates antihepatotoxic activity by reducing carbon tetrachloride and galactosamine-induced cytotoxicity in rat hepatocytes, indicating effectiveness at 1 mg/mL with GPT activity levels at 103.0% and 97.0% of the control, respectively. Although it shows no significant inhibitory activity against 5-lipoxygenase and COX1 (IC50 > 200,000 nM), it has notable agonist activity at human PR in HepG2 cells, enhancing MMTV gene promoter transactivation and luciferase activity at 10 µM and 100 µM. Conversely, it acts as an antagonist at human FXR, inhibiting CDCA-induced SHP gene transactivation in a dose-dependent manner (10 µM, 50 µM, 100 µM). In inflammatory models, it has weak antiinflammatory activity, reducing LPS-induced nitric oxide production in mouse RAW264.7 cells (IC50 > 100,000 nM). Neuroprotective effects are observed against glutamate-induced neuronal cell death in rat PC12 cells with an EC50 value of 36,300 nM. Additionally, Atractylenolide III inhibits sterol O-acyltransferase (SOAT) enzymes, showing varied IC50 values across different assays, including 211,000 nM in CHOK1 microsomes, and significant inhibition of cholesterol ester biosynthesis in CHO cells and microsomal fractions, with IC50 values ranging from 55,100 nM to over 195,000 nM..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Atractylenolide III (ICodonolactone) may have therapeutic potential in treating homocysteine-mediated cognitive impairment and neuronal injury. Atractylenolide III is a potential candidate for the treatment of human lung carcinoma by inducing the release of cytochrome c, upregulating the expression of Bax and translocating apoptosis-inducing factor.
SynonymsICodonolactone, 8β-Hydroxyasterolide
Chemical Properties
Molecular Weight248.32
FormulaC15H20O3
Cas No.73030-71-4
SmilesCC1=C2C[C@H]3C(=C)CCC[C@]3(C)C[C@]2(O)OC1=O
Relative Density.1.18 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
Chloroform, Dichloromethane, Ethyl Acetate, Acetone: Soluble
DMSO: 257.5 mg/mL (1036.97 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (8.05 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 mM4.0271 mL20.1353 mL40.2706 mL201.3531 mL
5 mM0.8054 mL4.0271 mL8.0541 mL40.2706 mL
10 mM0.4027 mL2.0135 mL4.0271 mL20.1353 mL
20 mM0.2014 mL1.0068 mL2.0135 mL10.0677 mL
50 mM0.0805 mL0.4027 mL0.8054 mL4.0271 mL
100 mM0.0403 mL0.2014 mL0.4027 mL2.0135 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:
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%
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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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