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Fidexaban
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Catalog No. T27318Cas No. 183305-24-0
Alias ZK-807834, PD-200022, CI-1031, CI1031, BX-807834, BX807834
Fidexaban (CI1031) is a novel, potent, selective and orally active factor Xa inhibitor that has demonstrated antithrombotic activity in a variety of assays
Fidexaban
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Purity: 99.43%
Catalog No. T27318Alias ZK-807834, PD-200022, CI-1031, CI1031, BX-807834, BX807834Cas No. 183305-24-0
Fidexaban (CI1031) is a novel, potent, selective and orally active factor Xa inhibitor that has demonstrated antithrombotic activity in a variety of assays
| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $143 | In Stock | In Stock | |
| 5 mg | $360 | In Stock | In Stock | |
| 10 mg | $530 | In Stock | In Stock | |
| 25 mg | $859 | In Stock | In Stock | |
| 50 mg | $1,180 | In Stock | In Stock | |
| 100 mg | $1,590 | - | In Stock |
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
This molecule is a custom-made product. TargetMol has an excellent synthesis team with the experience and capability to provide you with cost-effective products.If you have any questions, please feel free to contact us. We are committed to serving you wholeheartedly.
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.
Batch Information
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Purity:99.43%
Appearance:Solid
Color:White
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Product Introduction
Fidexaban AI Summary
Fidexaban exhibits a high inhibitory potency against human coagulation factor Xa with a Ki value of 0.11 nM. It also shows moderate inhibitory activity against bovine trypsin (Ki = 280.0 nM) and weaker activity against human thrombin (Ki = 2000.0 nM). The compound has good oral bioavailability in dogs and monkeys, with an F value of 20%. Pharmacokinetic studies in dogs after oral dosing show plasma concentrations of 3.0 µM at 1 hour, 2.1 µM at 2 hours, and 0.7 µM at 4 hours. In baboons, plasma concentrations range from 0.3 µM at 1 hour to 1.0 µM at 6 hours, while in cynomolgus monkeys, the concentrations range from 0.2 µM at 1 hour to 1.2 µM at 4 hours. Additionally, Fidexaban extends prothrombin time concentration by 230.0 nM..
Note: Summary generated by AI. Data source: ChEMBL 
Bioactivity
Chemical Properties
Storage & Solubility Information
| Description | Fidexaban (CI1031) is a novel, potent, selective and orally active factor Xa inhibitor that has demonstrated antithrombotic activity in a variety of assays |
| Targets&IC50 | FXa (human):0.11 nM(Ki) |
| In vitro | Fidexaban (ZK-807834) is a novel, synthetic factor Xa (FXa) inhibitor with a Ki of 0.11 nM against human FXa. In human plasma in vitro, Fidexaban doubled PT and aPTT at 0.23 and 0.49 microM, respectively. Ex vivo plasma anti-FXa activity was also well correlated with plasma concentration of Fidexaban and with PT (r = 0.96 and 0.98, respectively).[2] |
| Synonyms | ZK-807834, PD-200022, CI-1031, CI1031, BX-807834, BX807834 |
| Molecular Weight | 526.49 |
| Formula | C25H24F2N6O5 |
| Cas No. | 183305-24-0 |
| Smiles | O(C1=C(F)C(N(CC(O)=O)C)=C(F)C(OC2=CC(=CC=C2)C=3N(C)CCN3)=N1)C4=CC(C(=N)N)=CC=C4O |
| Relative Density. | 1.31g/cm3 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | H2O: < 1 mg/mL (insoluble or slightly soluble)  DMSO: < 1 mg/mL (insoluble or slightly soluble) |
Calculator
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:
For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, and a total of 10 animals are to be administered, using a formulation of 
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 DMSO 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 DMSO stock solution to 400 μL PEG300 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 ddH2O 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.
Dose Conversion
You can also refer to dose conversion for different animals. More Dose Conversion
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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