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Triadimefon

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Catalog No. T7726Cas No. 43121-43-3

Triadimefon is an azole fungicide used to control powdery mildew.

Triadimefon

Triadimefon

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Purity: 99.66%
Catalog No. T7726Cas No. 43121-43-3
Triadimefon is an azole fungicide used to control powdery mildew.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
200 mg$38In StockIn Stock
500 mg$59In StockIn Stock
1 g$71In StockIn Stock
5 g$168-In Stock
10 g$247-In Stock
1 mL x 10 mM (in DMSO)$46In 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:99.66%
Appearance:Solid
Color:White
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Product Introduction

Triadimefon AI Summary
Triadimefon exhibits a wide range of bioactivities including potent antifungal and antiviral properties. It displays significant antifungal activity against various pathogens such as Colletotrichum fragariae (zone of inhibition 121.0 mm), Helminthosporium sativum (MIC 20.0 µg/mL), Rhizoctonia solani (EC50 14.68 µg/mL), Botrytis cinerea, Gibberella zeae, Colletotrichum gossypii, and many others, with varying growth inhibition percentages from 35.0% to 95.0% at different concentrations. Furthermore, Triadimefon is a potent inhibitor of CYP3A4 with an IC50 value of 9289.66 nM and demonstrates binding affinity to Penicillium digitatum CYP51, with a Kd value of 935.5 nM. In plant protection, its antifungal efficacy has been noted against pathogens like Blumeria graminis f. sp. tritici, Venturia inaequalis, Bipolaris sorokiniana, and others, with considerable growth inhibition at concentrations as low as 50 ug/mL. Additionally, Triadimefon exhibits bioactivities in inhibiting SARS-CoV-2 3CL-Pro protease (22.22% inhibition at 20µM) and protecting VERO-6 cells from SARS-CoV-2-induced cytotoxicity, though requiring high concentrations (IC50 > 20,000 nM) for significant inhibition. Besides its antiviral and antifungal properties, it also influences various signaling pathways, such as being an activator and inhibitor in Cytochrome P450 3A4 activity, an agonist for estrogen receptor alpha, and an activator of the Aryl hydrocarbon receptor (AhR) signaling pathway..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Triadimefon is an azole fungicide used to control powdery mildew.
Chemical Properties
Molecular Weight293.75
FormulaC14H16ClN3O2
Cas No.43121-43-3
SmilesCC(C)(C)C(=O)C(Oc1ccc(Cl)cc1)n1cncn1
Relative Density.1.2200 g/cm3
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: 45 mg/mL (153.19 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.4043 mL17.0213 mL34.0426 mL170.2128 mL
5 mM0.6809 mL3.4043 mL6.8085 mL34.0426 mL
10 mM0.3404 mL1.7021 mL3.4043 mL17.0213 mL
20 mM0.1702 mL0.8511 mL1.7021 mL8.5106 mL
50 mM0.0681 mL0.3404 mL0.6809 mL3.4043 mL
100 mM0.0340 mL0.1702 mL0.3404 mL1.7021 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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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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