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KP496
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Catalog No. T11764Cas No. 217799-03-6
KP496 is a selective, dual antagonist for the Thromboxane A2 receptor (TP) and the Leukotriene D4 receptor (cysLT1).
KP496
😃Good
Catalog No. T11764Cas No. 217799-03-6
KP496 is a selective, dual antagonist for the Thromboxane A2 receptor (TP) and the Leukotriene D4 receptor (cysLT1).
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 25 mg | $1,820 | 8-10 weeks | 8-10 weeks | |
| 50 mg | $2,380 | 8-10 weeks | 8-10 weeks | |
| 100 mg | $3,100 | 8-10 weeks | 8-10 weeks |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Product Introduction
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | KP496 is a selective, dual antagonist for the Thromboxane A2 receptor (TP) and the Leukotriene D4 receptor (cysLT1). |
| In vivo | KP496 and prednisolone markedly reduce the rise in hydroxyl-L-proline levels in the lung, showing an inhibition ratio of approximately 74% and 63%, respectively, when compared to their own vehicle control groups. Both compounds at doses of KP496 (100 mg/head) and prednisolone (10 mg/kg) significantly decrease the infiltration of total cells, including eosinophils, monocytes/macrophages, and lymphocytes, relative to the control group. Additionally, KP496 at a lower dose (30mg/head) reduces the infiltration of these cell types, except for neutrophils, albeit not significantly. Furthermore, KP496 effectively curtails both acute (day 7) and chronic (day 21) lung inflammation, reducing lymphocyte numbers by day 7 and counts of macrophages, neutrophils, and eosinophils on days 7 and 21. |
| Molecular Weight | 692.27 |
| Formula | C31H34ClN3O7S3 |
| Cas No. | 217799-03-6 |
| Smiles | S(N(CC1=CC(OCC2=NC(C(C)C)=CS2)=CC=C1)CCCCNS(=O)(=O)C3=CC=C(Cl)C=C3)(=O)(=O)C4=C(C(O)=O)C=CC=C4 |
| Relative Density. | 1.378 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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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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