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Masilukast

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Catalog No. T27979Cas No. 136564-68-6
Alias ZD-3523, SA-09012, MCC-847, ICI-D-3523, ICI D-3523, D-3523

Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.

Masilukast

Masilukast

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🥰Excellent
Purity: 99.62%
Catalog No. T27979Alias ZD-3523, SA-09012, MCC-847, ICI-D-3523, ICI D-3523, D-3523Cas No. 136564-68-6
Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$316In StockIn Stock
5 mg$708In StockIn Stock
10 mg$948In StockIn Stock
25 mg$1,410In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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Purity:99.62%
ee:100%
Appearance:Solid
Color:White
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Product Introduction

Masilukast AI Summary
Masilukast exhibits bioactivity related to leukotriene receptors, specifically LTD4, with potent inhibition constants for displacing LTD4 on guinea pig lung parenchymal membranes and binding to LTE4 on guinea pig tracheal spirals. It effectively inhibits LTD4-induced dyspnea in guinea pigs via both oral and intravenous administration. The compound displays selectivity for receptors such as Thromboxane 2 and Prostaglandin 1. Additionally, its oral bioavailability and clearance rates have been evaluated in various animal models, including rats, guinea pigs, and dogs. Notably, the ratio of its effective doses administered orally versus intravenously is 52.0, indicating a significant difference in bioactivity depending on the route of administration..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Masilukast(MCC-847) is an oral leukotriene D4 (LTD4) receptor antagonist for the study of diseases associated with inflammation.
SynonymsZD-3523, SA-09012, MCC-847, ICI-D-3523, ICI D-3523, D-3523
Chemical Properties
Molecular Weight615.66
FormulaC31H32F3N3O5S
Cas No.136564-68-6
SmilesC(C=1C=2C(N(C)C1)=CC=C(C(NC[C@@H](CC(F)(F)F)C)=O)C2)C3=C(OC)C=C(C(NS(=O)(=O)C4=C(C)C=CC=C4)=O)C=C3
Relative Density.1.31g/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: 50 mg/mL (81.21 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.6243 mL8.1214 mL16.2427 mL81.2137 mL
5 mM0.3249 mL1.6243 mL3.2485 mL16.2427 mL
10 mM0.1624 mL0.8121 mL1.6243 mL8.1214 mL
20 mM0.0812 mL0.4061 mL0.8121 mL4.0607 mL
50 mM0.0325 mL0.1624 mL0.3249 mL1.6243 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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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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