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Heveadride
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Catalog No. TN11524Cas No. 39595-41-0
Heveadride is a fungal metabolite and antifungal agonist with activity against filamentous fungi and certain human pathogenic yeasts. It downregulates TNFα-induced NF-κB activity in human chronic leukemia cells, with an IC50 value of 82.7 μM.
Heveadride
😃Good
Catalog No. TN11524Cas No. 39595-41-0
Heveadride is a fungal metabolite and antifungal agonist with activity against filamentous fungi and certain human pathogenic yeasts. It downregulates TNFα-induced NF-κB activity in human chronic leukemia cells, with an IC50 value of 82.7 μM.
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Heveadride is a fungal metabolite and antifungal agonist with activity against filamentous fungi and certain human pathogenic yeasts. It downregulates TNFα-induced NF-κB activity in human chronic leukemia cells, with an IC50 value of 82.7 μM. |
| In vitro | Heveadride (Compound 2) exhibits moderate antifungal activity against filamentous fungi at concentrations of 5 and 10 μg/disc, shows no activity against yeast at 5 μg/disc, and demonstrates weak activity against some yeast strains at 100 μg/disc. Heveadride (Compound 4), at concentrations ranging from 10-100 μM over 2 hours, displays dose-dependent inhibition of TNFα-induced NF-κB activity in K562 cells. Heveadride, at concentrations of 0.1-100 μM for durations of 8-72 hours, does not significantly reduce K562 cell viability at any concentration or time point, but inhibits proliferation of K562 cells at 100 μM. |
| Molecular Weight | 332.35 |
| Formula | C18H20O6 |
| Cas No. | 39595-41-0 |
| Smiles | C(CC)[C@@H]1C2=C(CCC3=C(C[C@H]1CC)C(=O)OC3=O)C(=O)OC2=O |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
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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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