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(E)-[6]-Dehydroparadol

(E)-[6]-Dehydroparadol
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Purity:99.87%
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(E)-[6]-Dehydroparadol

Catalog No. T13436Cas No. 878006-06-5
(E)-[6]-Dehydroparadol ((6)-Dehydroparadol), an oxidative metabolite of [6]-Shogaol, is a potent Nrf2 activator.
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Pack SizePriceAvailabilityQuantity
1 mg$37In Stock
5 mg$85In Stock
10 mg$118In Stock
25 mg$218In Stock
50 mg$297In Stock
100 mg$428In Stock
500 mg$968In Stock
1 mL x 10 mM (in DMSO)$94In Stock
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Product Introduction

Bioactivity
Description
(E)-[6]-Dehydroparadol ((6)-Dehydroparadol), an oxidative metabolite of [6]-Shogaol, is a potent Nrf2 activator.
In vitro
(E)-[6]-Dehydroparadol (5-80 µM; 24 h) inhibits the growth of HCT-116 and H-1299 cells, with IC50s of 43.02 and 41.59 µM, respectively. (E)-[6]-Dehydroparadol (10-40 µM; 24 h) induces apoptosis in HCT-116 and H-1299 cells[1].
In vivo
(E)-[6]-Dehydroparadol at a concentration of 5 µM for 24 hours increases the fluorescence signal of Tg[glutathione S-transferase pi 1 (gstp1):green fluorescent protein (GFP)] in Tg(gstp1:GFP) transgenic zebrafish embryos.
Alias(6)-Dehydroparadol
Chemical Properties
Molecular Weight276.37
FormulaC17H24O3
Cas No.878006-06-5
Storage & Solubility Information
Storage Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 120 mg/mL (434.2 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.6183 mL18.0917 mL36.1834 mL180.9169 mL
5 mM0.7237 mL3.6183 mL7.2367 mL36.1834 mL
10 mM0.3618 mL1.8092 mL3.6183 mL18.0917 mL
20 mM0.1809 mL0.9046 mL1.8092 mL9.0458 mL
50 mM0.0724 mL0.3618 mL0.7237 mL3.6183 mL
100 mM0.0362 mL0.1809 mL0.3618 mL1.8092 mL

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TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLddH2OTargetMol | reagent mix well and clarify
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