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Milvexian (Synonyms: JNJ-70033093, BMS-986177)

Catalog No. T39223 Copy Product Info
Purity: 99.91%
🥰Excellent
Milvexian (BMS-986177/JNJ-70033093) is an orally bioavailable, small-molecule, reversible, and direct antagonist of Factor XIa (FXIa). It exhibits potent inhibitory activity across species, with Ki values of 0.11 nM for human, 0.38 nM for rabbit, and 0.64 nM for dog. By targeting FXIa, Milvexian selectively inhibits the intrinsic pathway of the coagulation cascade. It demonstrates robust antithrombotic efficacy in various in vitro and in vivo models while maintaining a favorable safety profile regarding bleeding risk. It is a critical tool for investigating novel anticoagulant strategies in thrombosis and cardiovascular research.

Milvexian

Copy Product Info
🥰Excellent
Catalog No. T39223
Synonyms JNJ-70033093, BMS-986177

Milvexian (BMS-986177/JNJ-70033093) is an orally bioavailable, small-molecule, reversible, and direct antagonist of Factor XIa (FXIa). It exhibits potent inhibitory activity across species, with Ki values of 0.11 nM for human, 0.38 nM for rabbit, and 0.64 nM for dog. By targeting FXIa, Milvexian selectively inhibits the intrinsic pathway of the coagulation cascade. It demonstrates robust antithrombotic efficacy in various in vitro and in vivo models while maintaining a favorable safety profile regarding bleeding risk. It is a critical tool for investigating novel anticoagulant strategies in thrombosis and cardiovascular research.

Milvexian
Cas No. 1802425-99-5
Pack SizePriceUSA StockGlobal StockQuantity
1 mg$496-In Stock
5 mg$993-In Stock
10 mg$1,490-In Stock
25 mg$2,680-In Stock
50 mg$3,760-In Stock
1 mL x 10 mM (in DMSO)$1,370-In Stock
For In stock only · Estimated delivery: USA Stock (1-2 days) Global Stock (5-7 days)
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Purity:99.91%
Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Milvexian (BMS-986177/JNJ-70033093) is an orally bioavailable, small-molecule, reversible, and direct antagonist of Factor XIa (FXIa). It exhibits potent inhibitory activity across species, with Ki values of 0.11 nM for human, 0.38 nM for rabbit, and 0.64 nM for dog. By targeting FXIa, Milvexian selectively inhibits the intrinsic pathway of the coagulation cascade. It demonstrates robust antithrombotic efficacy in various in vitro and in vivo models while maintaining a favorable safety profile regarding bleeding risk. It is a critical tool for investigating novel anticoagulant strategies in thrombosis and cardiovascular research.
In vitro
Milvexian (~10 μM) prolongs aPTT in human plasma, confirming selective blockade of the intrinsic coagulation pathway. It does not affect platelet aggregation induced by ADP or collagen, indicating that its antithrombotic effect is coagulation-specific, offering a mechanistic advantage in reducing bleeding risk [1].
In vivo
In a rabbit thrombosis model, Milvexian dose-dependently maintained carotid blood flow (32–76%) and reduced thrombus weight (15–70%) following i.v. administration. Orally dosed at 20 mg/kg, it achieved a plasma concentration of 2000 nM at 1 h, demonstrating favorable PK [1][2].
SynonymsJNJ-70033093, BMS-986177
Chemical Properties
Molecular Weight626.45
FormulaC28H23Cl2F2N9O2
Cas No.1802425-99-5
SmilesC(F)(F)N1C=2C=3C=C([C@H](CCC[C@@H](C)C(=O)NC2C=N1)N4C(=O)C=C(N=C4)C5=C(C=CC(Cl)=C5)N6C=C(Cl)N=N6)N=CC3
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: 80 mg/mL (127.7 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.5963 mL7.9815 mL15.9630 mL79.8148 mL
5 mM0.3193 mL1.5963 mL3.1926 mL15.9630 mL
10 mM0.1596 mL0.7981 mL1.5963 mL7.9815 mL
20 mM0.0798 mL0.3991 mL0.7981 mL3.9907 mL
50 mM0.0319 mL0.1596 mL0.3193 mL1.5963 mL
100 mM0.0160 mL0.0798 mL0.1596 mL0.7981 mL
Note : The dilution table applies only to solid products. For liquid products, please calculate the stock solution based on the stated concentration and/or density.

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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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%
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