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6-Dehydrogingerdione

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Catalog No. TN1171Cas No. 76060-35-0
Alias 1-Dehydro-6-gingerdione

6-Dehydrogingerdione sensitizes human hepatoblastoma Hep G2 cells to TRAIL-induced apoptosis via a reactive oxygen species-mediated mechanism that enhances DR5 expression, up-regulates Ser-15 phosphorylation, and triggers nuclear translocation of p53. Abrogation of p53 using small interfering RNA markedly reduces 6-Dehydrogingerdione-induced DR5 and diminishes TRAIL responsiveness. ROS generation accompanies DR5 activation, and pretreatment with N-acetyl-L-cysteine significantly attenuates these apoptotic responses, confirming 6-Dehydrogingerdione acts through p53-dependent and oxidative stress-mediated apoptotic pathways.

6-Dehydrogingerdione

6-Dehydrogingerdione

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Purity: 96.98%
Catalog No. TN1171Alias 1-Dehydro-6-gingerdioneCas No. 76060-35-0
6-Dehydrogingerdione sensitizes human hepatoblastoma Hep G2 cells to TRAIL-induced apoptosis via a reactive oxygen species-mediated mechanism that enhances DR5 expression, up-regulates Ser-15 phosphorylation, and triggers nuclear translocation of p53. Abrogation of p53 using small interfering RNA markedly reduces 6-Dehydrogingerdione-induced DR5 and diminishes TRAIL responsiveness. ROS generation accompanies DR5 activation, and pretreatment with N-acetyl-L-cysteine significantly attenuates these apoptotic responses, confirming 6-Dehydrogingerdione acts through p53-dependent and oxidative stress-mediated apoptotic pathways.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$147-In Stock
5 mg$372-In Stock
10 mg$548-In Stock
25 mg$869-In Stock
50 mg$1,170-In Stock
100 mg$1,570-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:96.98%
Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
6-Dehydrogingerdione sensitizes human hepatoblastoma Hep G2 cells to TRAIL-induced apoptosis via a reactive oxygen species-mediated mechanism that enhances DR5 expression, up-regulates Ser-15 phosphorylation, and triggers nuclear translocation of p53. Abrogation of p53 using small interfering RNA markedly reduces 6-Dehydrogingerdione-induced DR5 and diminishes TRAIL responsiveness. ROS generation accompanies DR5 activation, and pretreatment with N-acetyl-L-cysteine significantly attenuates these apoptotic responses, confirming 6-Dehydrogingerdione acts through p53-dependent and oxidative stress-mediated apoptotic pathways.
In vitro
6-Dehydrogingerdione (0-150 μM, 24 hours) induced apoptosis in Hep G2 cells in a dose-dependent manner [1].
Synonyms1-Dehydro-6-gingerdione
Chemical Properties
Molecular Weight290.35
FormulaC17H22O4
Cas No.76060-35-0
SmilesC(=C/C(CC(CCCCC)=O)=O)\C1=CC(OC)=C(O)C=C1
Relative Density.1.105 g/cm3 (Predicted)
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 (275.53 mM), Sonication is recommeded.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4441 mL17.2206 mL34.4412 mL172.2060 mL
5 mM0.6888 mL3.4441 mL6.8882 mL34.4412 mL
10 mM0.3444 mL1.7221 mL3.4441 mL17.2206 mL
20 mM0.1722 mL0.8610 mL1.7221 mL8.6103 mL
50 mM0.0689 mL0.3444 mL0.6888 mL3.4441 mL
100 mM0.0344 mL0.1722 mL0.3444 mL1.7221 mL

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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.
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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:

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