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Thiophanate-Methyl

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Catalog No. T6944Cas No. 23564-05-8

Thiophanate-Methyl (TM), a methyl benzimidazole carbamate (MBC) fungicide,

Thiophanate-Methyl

Thiophanate-Methyl

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🥰Excellent
Purity: 99.58%
Catalog No. T6944Cas No. 23564-05-8
Thiophanate-Methyl (TM), a methyl benzimidazole carbamate (MBC) fungicide,
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
500 mg$31In StockIn Stock
1 g$52In StockIn Stock
1 mL x 10 mM (in DMSO)$35In 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:99.58%
Appearance:Solid
Color:White
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Product Introduction

Thiophanate-Methyl AI Summary
Thiophanate-Methyl exhibits a broad range of bioactivities, including notable antifungal, antiviral, and enzyme-inhibitory properties. It demonstrates substantial antifungal activity against a variety of pathogens, such as Colletotrichum fragariae, Fusarium oxysporum, Pestalotiopsis microspora, and Thanatephorus cucumeris, with significant inhibitory effects on mycelial growth, conidium germination, and disease control in plants. Specifically, it inhibits mycelial growth with Minimum Inhibitory Concentration (MIC) values of 4000.0 ppm for Cochliobolus pallescens, Fusarium oxysporum, and Glomerella tucumanensis, and shows an EC50 as low as 10.84 ug/mL against Rhizoctonia solani AG-1 IA and 1.03 ug/mL against Botryotinia fuckeliana. In addition to its antifungal properties, Thiophanate-Methyl has antiviral activity against SARS-CoV-2, inhibiting cytotoxicity in Caco-2 and VERO-6 cells at a concentration of 10 uM and demonstrating -3.43% and 0.14% inhibition respectively. It also inhibits the SARS-CoV-2 3CL-Pro protease by 11.73% at 20 µM. Enzyme inhibition studies reveal that Thiophanate-Methyl is a potent inhibitor of various enzymes including HSD17B4, ALDH1A1, and Bacillus subtilis Sfp PPTase, with potencies ranging from 316.2 nM to 50118.7 nM. It also inhibits human FAAH at 1 uM with an 8.37% inhibition rate, and HDAC6 enzyme with mixed results depending on the substrate used. Overall, Thiophanate-Methyl displays a diverse spectrum of biological activities, making it a promising candidate for further research in antifungal therapy, antiviral treatment, and enzyme inhibition applications..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Thiophanate-Methyl (TM), a methyl benzimidazole carbamate (MBC) fungicide,
Chemical Properties
Molecular Weight342.39
FormulaC12H14N4O4S2
Cas No.23564-05-8
SmilesCOC(=O)NC(=S)Nc1ccccc1NC(=S)NC(=O)OC
Relative Density.1.4542 g/cm3 (Estimated)
Storage & Solubility Information
Storagekeep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 83.33 mg/mL (243.38 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 5 mg/mL (14.6 mM), Sonication is recommended.
Please add the solvents sequentially, clarifying the solution as much as possible before adding the next one. Dissolve by heating and/or sonication if necessary. Working solution is recommended to be prepared and used immediately. The formulation provided above is for reference purposes only. In vivo formulations may vary and should be modified based on specific experimental conditions.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9206 mL14.6032 mL29.2065 mL146.0323 mL
5 mM0.5841 mL2.9206 mL5.8413 mL29.2065 mL
10 mM0.2921 mL1.4603 mL2.9206 mL14.6032 mL
20 mM0.1460 mL0.7302 mL1.4603 mL7.3016 mL
50 mM0.0584 mL0.2921 mL0.5841 mL2.9206 mL
100 mM0.0292 mL0.1460 mL0.2921 mL1.4603 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:
% 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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