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Etalocib

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Catalog No. T22358Cas No. 161172-51-6
Alias VML295, LY293111

Etalocib (LY293111) is a novel diaryl ether carboxylic acid derivative, is a selective and potent inhibitor of the lipoxygenase pathway either via antagonism of the leukotriene B4 (LTB4) receptor or directly through 5'-lipoxygenase. It has antineoplastic activities.

Etalocib

Etalocib

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Purity: 98.21%
Catalog No. T22358Alias VML295, LY293111Cas No. 161172-51-6
Etalocib (LY293111) is a novel diaryl ether carboxylic acid derivative, is a selective and potent inhibitor of the lipoxygenase pathway either via antagonism of the leukotriene B4 (LTB4) receptor or directly through 5'-lipoxygenase. It has antineoplastic activities.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$65In StockIn Stock
5 mg$163In StockIn Stock
10 mg$238In StockIn Stock
25 mg$442In StockIn Stock
50 mg$648In StockIn Stock
100 mg$930In StockIn Stock
200 mg$1,250-In Stock
1 mL x 10 mM (in DMSO)$203In 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:98.21%
Appearance:Solid
Color:White
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Product Introduction

Etalocib AI Summary
Etalocib shows significant bioactivities as an inhibitor of leukotriene B4 (LTB4) receptors and related pathways. It displays a high binding affinity towards human neutrophil LTB4 receptors with a Ki of 25.0 nM and against guinea pig lung membrane LTB4 receptors with a Ki of 6.6 nM. The compound also inhibits LTB4-induced calcium mobilization with an IC50 of 20.0 nM. Additionally, it effectively inhibits the expression of human neutrophil integrin CD11b/CD18 with an IC50 of around 3.9 nM in one study and 3.3 nM in another. In vivo studies demonstrated its inhibitory effects on LTB4-induced bronchoconstriction with an ED50 of 0.04 mg/kg intravenously and 0.4 mg/kg orally. These findings suggest potential anti-inflammatory properties of Etalocib through its interactions with LTB4 receptors..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
Etalocib (LY293111) is a novel diaryl ether carboxylic acid derivative, is a selective and potent inhibitor of the lipoxygenase pathway either via antagonism of the leukotriene B4 (LTB4) receptor or directly through 5'-lipoxygenase. It has antineoplastic activities.
SynonymsVML295, LY293111
Chemical Properties
Molecular Weight544.6
FormulaC33H33FO6
Cas No.161172-51-6
SmilesCCCc1c(OCCCOc2cc(O)c(cc2CC)-c2ccc(F)cc2)cccc1Oc1ccccc1C(O)=O
Relative Density.1.215g/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: 100 mg/mL (183.62 mM), Sonication is recommended.
In Vivo Formulation
10% DMSO+90% Corn Oil: 3.3 mg/mL (6.06 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 mM1.8362 mL9.1811 mL18.3621 mL91.8105 mL
5 mM0.3672 mL1.8362 mL3.6724 mL18.3621 mL
10 mM0.1836 mL0.9181 mL1.8362 mL9.1811 mL
20 mM0.0918 mL0.4591 mL0.9181 mL4.5905 mL
50 mM0.0367 mL0.1836 mL0.3672 mL1.8362 mL
100 mM0.0184 mL0.0918 mL0.1836 mL0.9181 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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