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Firocoxib

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Catalog No. T7596Cas No. 189954-96-9
Alias ML 1785713

Firocoxib (ML 1785713) is a selective non-steroidal inhibitor of cyclooxygenase-2 (COX-2) with an IC50 of 0.13 μM, used for its anti-inflammatory properties in dogs and horses.

Firocoxib

Firocoxib

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Purity: 99.84%
Catalog No. T7596Alias ML 1785713Cas No. 189954-96-9
Firocoxib (ML 1785713) is a selective non-steroidal inhibitor of cyclooxygenase-2 (COX-2) with an IC50 of 0.13 μM, used for its anti-inflammatory properties in dogs and horses.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$33In StockIn Stock
5 mg$68In StockIn Stock
10 mg$111In StockIn Stock
25 mg$215In StockIn Stock
50 mg$318In StockIn Stock
100 mg$477In StockIn Stock
1 mL x 10 mM (in DMSO)$77In 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:99.84%
Appearance:Solid
Color:White
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Product Introduction

Firocoxib AI Summary
Firocoxib exhibits potent inhibition of Prostaglandin G/H synthase 2 activity in human whole blood, with an IC50 value of 140.0 nM, while demonstrating weak inhibition against Prostaglandin G/H synthase 1, with an IC50 value greater than 100000.0 nM. It shows moderate activity in a U937 Microsome COX-1 assay, with an IC50 value of 25000.0 nM. In addition to its anti-inflammatory properties, Firocoxib has shown antiviral activities against SARS-CoV-2. It inhibits SARS-CoV-2 induced cytotoxicity in Caco-2 cells at a concentration of 10 μM after 48 hours, with an inhibition rate of 3.46%. Against the USA-WA1/2020 strain in HRCE cells, it yielded a hit score of 0.09893 at MOI 0.4 after 96 hours. The compound also inhibits SARS-CoV-2 3CL-Pro protease activity by 0.5656% at a 20μM concentration. However, high content imaging of virus-induced cytotoxicity in VERO-6 cells at 10 μM after 48 hours showed an inhibition of -0.04%. Additionally, Firocoxib exhibits inhibitory activity against human HDAC6, with inhibition percentages of -6.89% and -3.0% in enzymatic assays using commercial and custom peptide substrates, respectively..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Firocoxib (ML 1785713) is a selective non-steroidal inhibitor of cyclooxygenase-2 (COX-2) with an IC50 of 0.13 μM, used for its anti-inflammatory properties in dogs and horses.
Targets&IC50
COX-2:0.13 μM, COX-1:7.5 μM
SynonymsML 1785713
Chemical Properties
Molecular Weight336.4
FormulaC17H20O5S
Cas No.189954-96-9
SmilesO(CC1CC1)C2=C(C(C)(C)OC2=O)C3=CC=C(S(C)(=O)=O)C=C3
Relative Density.1.31 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: 47 mg/mL (139.71 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.9727 mL14.8633 mL29.7265 mL148.6326 mL
5 mM0.5945 mL2.9727 mL5.9453 mL29.7265 mL
10 mM0.2973 mL1.4863 mL2.9727 mL14.8633 mL
20 mM0.1486 mL0.7432 mL1.4863 mL7.4316 mL
50 mM0.0595 mL0.2973 mL0.5945 mL2.9727 mL
100 mM0.0297 mL0.1486 mL0.2973 mL1.4863 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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