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Zaurategrast

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Catalog No. T17286Cas No. 455264-31-0
Alias Zaurategrast, CT-7758, CT7758, CT 7758

Zaurategrast (CDP323) is a small-molecule prodrug antagonist that inhibits the interaction between vascular cell adhesion molecule 1 (VCAM-1) and α4-integrins, originally developed by Celltech plc for oral administration, and it serves as a valuable research compound for investigating leukocyte trafficking, immune cell adhesion, and therapeutic strategies relevant to multiple sclerosis.

Zaurategrast

Zaurategrast

😃Good
Catalog No. T17286Alias Zaurategrast, CT-7758, CT7758, CT 7758Cas No. 455264-31-0
Zaurategrast (CDP323) is a small-molecule prodrug antagonist that inhibits the interaction between vascular cell adhesion molecule 1 (VCAM-1) and α4-integrins, originally developed by Celltech plc for oral administration, and it serves as a valuable research compound for investigating leukocyte trafficking, immune cell adhesion, and therapeutic strategies relevant to multiple sclerosis.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$69-In Stock
5 mgPreferential-In 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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Appearance:Solid
Color:Yellow
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Product Introduction

Bioactivity
Description
Zaurategrast (CDP323) is a small-molecule prodrug antagonist that inhibits the interaction between vascular cell adhesion molecule 1 (VCAM-1) and α4-integrins, originally developed by Celltech plc for oral administration, and it serves as a valuable research compound for investigating leukocyte trafficking, immune cell adhesion, and therapeutic strategies relevant to multiple sclerosis.
Targets&IC50
α4-integrin:< 100 nM
In vitro
Method: Pharmacokinetic properties of Zaurategrast were assessed using in vitro permeability and uptake assays and in vivo studies in mice, rats, dogs, and cynomolgus monkeys, followed by evaluation of an ethyl ester prodrug.
Result: Zaurategrast showed low oral bioavailability in rodents and monkeys due to poor absorption and active hepatic uptake, while the prodrug CDP323 improved permeability and oral bioavailability with effective in vivo conversion[1].
SynonymsZaurategrast, CT-7758, CT7758, CT 7758
Chemical Properties
Molecular Weight521.41
FormulaC26H25BrN4O3
Cas No.455264-31-0
SmilesN([C@@H](CC1=CC=C(NC=2C3=C(C=CN2)C=CN=C3)C=C1)C(O)=O)C=4C5(C(=O)C4Br)CCCCC5
Relative Density.1.31g/cm3
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 80 mg/mL (153.43 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9179 mL9.5894 mL19.1788 mL95.8938 mL
5 mM0.3836 mL1.9179 mL3.8358 mL19.1788 mL
10 mM0.1918 mL0.9589 mL1.9179 mL9.5894 mL
20 mM0.0959 mL0.4795 mL0.9589 mL4.7947 mL
50 mM0.0384 mL0.1918 mL0.3836 mL1.9179 mL
100 mM0.0192 mL0.0959 mL0.1918 mL0.9589 mL

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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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