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Epoxiconazole

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Catalog No. T19721Cas No. 133855-98-8
Alias EC-406-850-2, EC 406 850 2, BAS-480F, BAS480F, BAS 480F

Epoxiconazole (BAS-480F) is a 14-α demethylase inhibitor. It inhibits ergosterol synthesis and fungal cell wall formation.

Epoxiconazole

Epoxiconazole

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Purity: 98.57%
Catalog No. T19721Alias EC-406-850-2, EC 406 850 2, BAS-480F, BAS480F, BAS 480FCas No. 133855-98-8
Epoxiconazole (BAS-480F) is a 14-α demethylase inhibitor. It inhibits ergosterol synthesis and fungal cell wall formation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
10 mg$41In StockIn Stock
25 mg$74In StockIn Stock
50 mg$97In StockIn Stock
100 mg$157In StockIn Stock
200 mg$237-In Stock
1 mL x 10 mM (in DMSO)$30In 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:98.57%
Appearance:Solid
Color:White
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Product Introduction

Epoxiconazole AI Summary
Epoxiconazole exhibits broad-spectrum antifungal activity, targeting a variety of fungal pathogens including Fusarium graminearum, Zymoseptoria tritici, Oculimacula yallundae, and Oculimacula acuformis. Against Fusarium graminearum, it shows significant growth inhibition at a concentration of 10^-4 M after 14 days and notable antifungal activity within 8 hours, with an EC50 value of 10800000.0 nM. For Zymoseptoria tritici, EC50 values range from 0.0015 to 1.41 ug/mL, demonstrating variable potency across different strains and genetic backgrounds. Furthermore, it effectively inhibits germ tube elongation and mycelial growth of Oculimacula species, including resistant strains, with a higher selectivity towards Oculimacula acuformis. The compound also has a low toxicity profile in Rattus norvegicus (LD50 of 3160.0 mg.kg^-1) and exhibits low solubility at 0.7 mg per 100 g. Overall, Epoxiconazole holds promise for controlling a wide range of fungal pathogens, including those resistant to other fungicidal agents..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Epoxiconazole (BAS-480F) is a 14-α demethylase inhibitor. It inhibits ergosterol synthesis and fungal cell wall formation.
SynonymsEC-406-850-2, EC 406 850 2, BAS-480F, BAS480F, BAS 480F
Chemical Properties
Molecular Weight329.76
FormulaC17H13ClFN3O
Cas No.133855-98-8
SmilesFc1ccc(cc1)[C@@]1(Cn2cncn2)O[C@@H]1c1ccccc1Cl
Relative Density.1.39 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 142.8 mg/mL (433.04 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.0325 mL15.1625 mL30.3251 mL151.6254 mL
5 mM0.6065 mL3.0325 mL6.0650 mL30.3251 mL
10 mM0.3033 mL1.5163 mL3.0325 mL15.1625 mL
20 mM0.1516 mL0.7581 mL1.5163 mL7.5813 mL
50 mM0.0607 mL0.3033 mL0.6065 mL3.0325 mL
100 mM0.0303 mL0.1516 mL0.3033 mL1.5163 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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