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Chloranil

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Catalog No. T80673Cas No. 118-75-2
Alias p-Chloranil

Chloranil (tetrachloro-p-benzoquinone) triggers inflammation and neurological dysfunction through Toll-like receptor 4 signaling and can be used to model inflammation in mice.

Chloranil

Chloranil

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Purity: 98.03%
Catalog No. T80673Alias p-ChloranilCas No. 118-75-2
Chloranil (tetrachloro-p-benzoquinone) triggers inflammation and neurological dysfunction through Toll-like receptor 4 signaling and can be used to model inflammation in mice.
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1 g$29In 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:98.03%
Appearance:Solid
Color:Yellow
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Product Introduction

Chloranil AI Summary
Chloranil exhibits notable bioactivity across a variety of biological targets and pathogens. It functions as an inhibitor of several esterases and cholinesterases, with inhibition constants (Ki) of 57.4 nM, 83.9 nM, and 54.8 nM against human intestinal carboxylesterase 2, human liver carboxylesterase 1, and rabbit liver carboxylesterase, respectively. It also inhibits human Acetylcholinesterase and Butyrylcholinesterase with Ki values of 163.0 nM and 268.0 nM. Additionally, Chloranil shows antiparasitic activity against Trichomonas vaginalis strains T1 and G3 with 12.0% and 40.0% inhibition at 100 µM, respectively. The compound demonstrates cytotoxicity against cancer cells and inhibition of cellular functions such as DNA helicase, hormone receptors, and kinase signaling pathways. It exhibits toxicity against Trichoplusia ni larvae with a 10.0% mortality rate at 10 µg/ml and a feeding deterrence effect of 35.8% at 50 µg/cm². In cellular transport assays, Chloranil inhibits the uptake of sodium fluorescein in OATP1B3- and OATP1B1-transfected CHO cells by 74.83% and 80.53%, respectively. Remarkably, Chloranil has antimalarial activity against chloroquine-sensitive Plasmodium falciparum with an IC50 of 22400.0 nM and a selectivity index greater than 4.4 against human MRC5 cells. It strongly inhibits the refolding activity of GroEL/GroES proteins in Escherichia coli, resulting in a 92.0% reduction in enzyme activity in both rhodanese and soluble pig heart MDH assays. In addition to its enzymatic inhibition properties, Chloranil exhibits significant antiviral activity against SARS-CoV-2. It inhibits the SARS-CoV-2 3CL-Pro protease with an IC50 of less than 20.0 nM, achieving 102.77% inhibition at 20 µM. Moreover, it reduces SARS-CoV-2 induced cytotoxicity in VERO-6 cells, though its IC50 values in this context are greater than 20000.0 nM. Notably, the compound also shows inhibition in FRET-based protease assays with an IC50 of less than 0.02 µM. Overall, Chloranil is a versatile bioactive molecule with potential applications in combating diseases caused by different pathogens, including parasites and viruses, as well as being useful in enzymatic inhibition and cytotoxicity assays..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Chloranil (tetrachloro-p-benzoquinone) triggers inflammation and neurological dysfunction through Toll-like receptor 4 signaling and can be used to model inflammation in mice.
Synonymsp-Chloranil
Chemical Properties
Molecular Weight245.88
FormulaC6Cl4O2
Cas No.118-75-2
SmilesClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O
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: 50 mg/mL (203.35 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM4.0670 mL20.3351 mL40.6702 mL203.3512 mL
5 mM0.8134 mL4.0670 mL8.1340 mL40.6702 mL
10 mM0.4067 mL2.0335 mL4.0670 mL20.3351 mL
20 mM0.2034 mL1.0168 mL2.0335 mL10.1676 mL
50 mM0.0813 mL0.4067 mL0.8134 mL4.0670 mL
100 mM0.0407 mL0.2034 mL0.4067 mL2.0335 mL

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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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