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IDOR-1117-2520

Catalog No. T86705 Copy Product Info
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IDOR-1117-2520 is a potent and selective CCR6 antagonist that effectively blocks CCL20-mediated calcium signaling and inhibits β-arrestin recruitment in human CCR6-expressing cells, thereby serving as a valuable pharmacological agent for investigating CCR6-driven immune cell migration and autoimmune disease mechanisms.

IDOR-1117-2520

Copy Product Info
🥰Excellent
Catalog No. T86705

IDOR-1117-2520 is a potent and selective CCR6 antagonist that effectively blocks CCL20-mediated calcium signaling and inhibits β-arrestin recruitment in human CCR6-expressing cells, thereby serving as a valuable pharmacological agent for investigating CCR6-driven immune cell migration and autoimmune disease mechanisms.

IDOR-1117-2520
Cas No. 2737274-49-4
Pack SizePriceUSA StockGlobal StockQuantity
25 mg$2,570-In Stock
50 mg$3,360-In Stock
100 mg$4,210-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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For research use only—not for human use. No sales to individuals. Use as intended only.
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Product Introduction

Bioactivity
Description
IDOR-1117-2520 is a potent and selective CCR6 antagonist that effectively blocks CCL20-mediated calcium signaling and inhibits β-arrestin recruitment in human CCR6-expressing cells, thereby serving as a valuable pharmacological agent for investigating CCR6-driven immune cell migration and autoimmune disease mechanisms.
In vivo
In the context of autoimmune disease models, IDOR-1117-2520 is evaluated for its ability to mitigate tissue inflammation. By preventing the infiltration of pathogenic Th17 cells into inflamed tissues, the compound aims to dampen the autoimmune response and reduce pathology. This mechanism is investigated in preclinical models of autoimmunity, such as skin inflammation (psoriasis) or intestinal inflammation (IBD) [1].
Chemical Properties
Molecular Weight436.55
FormulaC25H32N4O3
Cas No.2737274-49-4
Smiles[C@](O)(C1(C)CN(C)C1)(C=2C=C(C=NC2)C=3N=C(C(C)(C)O)ON3)C4=CC=C(C(C)C)C=C4
Storage & Solubility Information
StorageShipping with blue ice.

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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:
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2 Enter the in vivo formulation:
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