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Foropafant

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Catalog No. T15338Cas No. 136468-36-5
Alias SR27417

Foropafant (SR27417) is a highly potent and selective platelet-activating factor (PAF) receptor antagonist (Ki: 57 pM). Foropafant potently inhibits the PAF-induced aggregation of rabbit and human platelets.

Foropafant

Foropafant

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Purity: 99.67%
Catalog No. T15338Alias SR27417Cas No. 136468-36-5
Foropafant (SR27417) is a highly potent and selective platelet-activating factor (PAF) receptor antagonist (Ki: 57 pM). Foropafant potently inhibits the PAF-induced aggregation of rabbit and human platelets.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$35In StockIn Stock
5 mg$81In StockIn Stock
10 mg$139In StockIn Stock
25 mg$320In StockIn Stock
50 mg$461In StockIn Stock
100 mg$648In StockIn Stock
1 mL x 10 mM (in DMSO)$83In 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:99.67%
Appearance:Solid
Color:Yellow
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Product Introduction

Foropafant AI Summary
Foropafant exhibits antiviral activity against SARS-CoV-2 by inhibiting virus-induced cytotoxicity in both Caco-2 and VERO-6 cells at a concentration of 10 µM after 48 hours. The inhibition rates were -2.37% and -0.06%, respectively. Additionally, Foropafant shows 7.093% inhibition of SARS-CoV-2 3CL-Pro protease at a 20 µM concentration, indicating potential bioactivity in blocking a crucial enzyme for viral replication. Moreover, the compound displays mixed bioactivities in the enzymatic assay of human HDAC6, with 1.94% inhibition using a commercial peptide substrate and -8.9% inhibition using a custom peptide substrate. These findings suggest that Foropafant has multifaceted interactions with various viral and human proteins, supporting its potential as an antiviral agent..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Foropafant (SR27417) is a highly potent and selective platelet-activating factor (PAF) receptor antagonist (Ki: 57 pM). Foropafant potently inhibits the PAF-induced aggregation of rabbit and human platelets.
Targets&IC50
PAF:57 pM (Ki)
SynonymsSR27417
Chemical Properties
Molecular Weight464.71
FormulaC28H40N4S
Cas No.136468-36-5
SmilesCC(C)c1cc(C(C)C)c(-c2csc(n2)N(CCN(C)C)Cc2cccnc2)c(c1)C(C)C
Relative Density.1.065 g/cm3 (Predicted)
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 (107.59 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (4.3 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 mM2.1519 mL10.7594 mL21.5188 mL107.5940 mL
5 mM0.4304 mL2.1519 mL4.3038 mL21.5188 mL
10 mM0.2152 mL1.0759 mL2.1519 mL10.7594 mL
20 mM0.1076 mL0.5380 mL1.0759 mL5.3797 mL
50 mM0.0430 mL0.2152 mL0.4304 mL2.1519 mL
100 mM0.0215 mL0.1076 mL0.2152 mL1.0759 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

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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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