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GW 766994

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Catalog No. T11521Cas No. 408303-43-5
Alias GW994, GW766994, GW 994

GW 766994 is a selective, orally active CCR3 (chemokine receptor-3) antagonist (Ki=13.8 nM) with anti-inflammatory effects, suitable for studying asthma and eosinophilic bronchitis.

GW 766994

GW 766994

😃Good
Purity: 98.77%
Catalog No. T11521Alias GW994, GW766994, GW 994Cas No. 408303-43-5
GW 766994 is a selective, orally active CCR3 (chemokine receptor-3) antagonist (Ki=13.8 nM) with anti-inflammatory effects, suitable for studying asthma and eosinophilic bronchitis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
25 mg$1,2006-8 weeks6-8 weeks
50 mg$1,5606-8 weeks6-8 weeks
100 mg$2,5006-8 weeks6-8 weeks
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Purity:98.77%
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Product Introduction

Bioactivity
Description
GW 766994 is a selective, orally active CCR3 (chemokine receptor-3) antagonist (Ki=13.8 nM) with anti-inflammatory effects, suitable for studying asthma and eosinophilic bronchitis.
Targets&IC50
CCR3:7.86 (pki)
In vitro
CCL11 treatment leads to the activation of CDK5 and GSK3β in hippocampal neurons, increased phosphorylation of tau protein at multiple sites, significantly elevated secretion of Aβ1-42, and a marked reduction in dendritic spine density. These effects were blocked by the CCR3-specific antagonist GW 766994 (10 μM) [2].
SynonymsGW994, GW766994, GW 994
Chemical Properties
Molecular Weight451.35
FormulaC21H24Cl2N4O3
Cas No.408303-43-5
SmilesNC(=O)c1ccc(CNC(=O)NC[C@H]2CN(Cc3ccc(Cl)c(Cl)c3)CCO2)cc1
Relative Density.1.331 g/cm3 (Predicted)
ColorWhite
AppearanceSolid
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: 40 mg/mL (88.62 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+40% PEG300+5% Tween-80+45% Saline: 2 mg/mL (4.43 mM), Sonication is recommeded.
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 mM2.2156 mL11.0779 mL22.1558 mL110.7788 mL
5 mM0.4431 mL2.2156 mL4.4312 mL22.1558 mL
10 mM0.2216 mL1.1078 mL2.2156 mL11.0779 mL
20 mM0.1108 mL0.5539 mL1.1078 mL5.5389 mL
50 mM0.0443 mL0.2216 mL0.4431 mL2.2156 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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