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Thiohexam

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Catalog No. T9037Cas No. 95-33-0

Thiohexam is a rubber vulcanization accelerator

Thiohexam

Thiohexam

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Purity: 97.33%
Catalog No. T9037Cas No. 95-33-0
Thiohexam is a rubber vulcanization accelerator
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 g$31In StockIn Stock
5 g$64-In Stock
10 g$98-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:97.33%
Appearance:Solid
Color:White
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Product Introduction

Thiohexam AI Summary
Thiohexam exhibits a wide range of bioactivities, particularly as an inhibitor in various biochemical and cellular assays. It is a potent inhibitor of ALDH1A1 with an IC50 of 794.3 nM, G9a histone lysine methyltransferase at 1778.3 nM, ROR gamma transcriptional activity at 8912.5 nM, and the vitamin D receptor (VDR) with a potency of 10000.0 nM. Additionally, it inhibits TDP1 in vitro with an IC50 of 39810.7 nM and in cells in the absence of CPT with an IC50 of 16788.9 nM, among other targets. The compound demonstrates cytotoxic activity against SH-SY5Y, HepG2, and MCF7 cells with IC50 values greater than 120000.0 nM, 55000.0 nM, and 89200.0 nM, respectively, indicating varying degrees of cell viability inhibition. Furthermore, Thiohexam has shown significant antiviral activity by reducing SARS-CoV-2 induced cytotoxicity in Caco-2 cells by 26.21% at 10 µM, and in VERO-6 cells with an inhibition rate of 0.03% at the same concentration. Notably, Thiohexam is a strong inhibitor of the SARS-CoV-2 3CL-Pro protease with an IC50 of 770.0 nM and demonstrates 24.67% inhibition at 20 µM, although it is much less effective against the MERS 3CL-Pro protease, with no observed inhibition at 10 µM and an IC50 greater than 10000.0 nM. Additionally, the compound shows mixed results in HDAC6 enzyme inhibition assays: 80.03% inhibition in an enzymatic assay with a commercial peptide substrate, -3.25% inhibition with a custom peptide substrate, and 23.24% inhibition in a hit confirmation assay using a custom peptide substrate..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Thiohexam is a rubber vulcanization accelerator
Chemical Properties
Molecular Weight264.41
FormulaC13H16N2S2
Cas No.95-33-0
SmilesC1CCC(CC1)NSc1nc2ccccc2s1
Relative Density.1.31~1.34g/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: 22.5 mg/mL (85.1 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM3.7820 mL18.9100 mL37.8201 mL189.1003 mL
5 mM0.7564 mL3.7820 mL7.5640 mL37.8201 mL
10 mM0.3782 mL1.8910 mL3.7820 mL18.9100 mL
20 mM0.1891 mL0.9455 mL1.8910 mL9.4550 mL
50 mM0.0756 mL0.3782 mL0.7564 mL3.7820 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

You can also refer to dose conversion for different animals. More Dose Conversion

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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