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CAY10471 Racemate

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Catalog No. T7359Cas No. 844639-57-2
Alias TM30089 Racemate

CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective CRTH2/DP2 receptor antagonist. It binds to human CRTH2/DP2, DP1, and TP receptors with Ki values of 0.6, 1200, and >10,000 nM, respectively.

CAY10471 Racemate

CAY10471 Racemate

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Purity: 99.08%
Catalog No. T7359Alias TM30089 RacemateCas No. 844639-57-2
CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective CRTH2/DP2 receptor antagonist. It binds to human CRTH2/DP2, DP1, and TP receptors with Ki values of 0.6, 1200, and >10,000 nM, respectively.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
5 mg$43In StockIn Stock
10 mg$68In StockIn Stock
25 mg$143In StockIn Stock
50 mg$213In StockIn Stock
100 mg$316In StockIn Stock
200 mg$457-In Stock
1 mL x 10 mM (in DMSO)$47In StockIn Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:99.08%
Appearance:Solid
Color:White
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Product Introduction

CAY10471 Racemate AI Summary
CAY10471 Racemate displays a high binding affinity for the human recombinant CRTH2 receptor with a Ki of 6.0 nM and an IC50 value of 3.6 nM, indicating potential activity in modulating allergic responses mediated by this receptor. It also exhibits moderate binding affinity to the prostanoid DP1 receptor with a Ki of 653.0 nM and to the thromboxane receptor with a Ki of 1394.0 nM, while showing low affinity for the TP receptor with a Ki value greater than 10000.0 nM. Additionally, the compound has been shown to inhibit the proliferation of Plasmodium falciparum (DD2) with a potency of 7492.9 nM according to PubChem BioAssay qHTS profiling. Incucyte cell viability assays reveal moderate to high growth rates in U2OS cells, ranging from 0.61 to 0.93, and variable effects on human fibroblast cells, reflecting complex interactions with different cell types. Furthermore, thermal shift assay results indicate diverse effects on the thermal stability of various protein domains, suggesting interactions that may modulate protein function or structure. These bioactivity results support the potential pharmacological interest of CAY10471 Racemate in anti-inflammatory, anti-malarial, and possibly other therapeutic areas..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
CAY10471 Racemate (TM30089 Racemate) is a potent and highly selective CRTH2/DP2 receptor antagonist. It binds to human CRTH2/DP2, DP1, and TP receptors with Ki values of 0.6, 1200, and >10,000 nM, respectively.
Targets&IC50
CRTH2:0.6 nM(ki) , DP:1200 nM(ki)
SynonymsTM30089 Racemate
Chemical Properties
Molecular Weight416.47
FormulaC21H21FN2O4S
Cas No.844639-57-2
Smiles[Na+].CN(C1CCc2c(C1)c1ccccc1n2CC([O-])=O)S(=O)(=O)c1ccc(F)cc1
Relative Density.1.41 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: 150 mg/mL (360.17 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween 80+45% Saline: 4 mg/mL (9.6 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 mM2.4011 mL12.0057 mL24.0113 mL120.0567 mL
5 mM0.4802 mL2.4011 mL4.8023 mL24.0113 mL
10 mM0.2401 mL1.2006 mL2.4011 mL12.0057 mL
20 mM0.1201 mL0.6003 mL1.2006 mL6.0028 mL
50 mM0.0480 mL0.2401 mL0.4802 mL2.4011 mL
100 mM0.0240 mL0.1201 mL0.2401 mL1.2006 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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