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PPACK Dihydrochloride (Synonyms: Pebac dihydrochloride, D-Phe-Pro-Arg-CH2Cl 2HCl, D-Phenylalanyl-prolyl-arginy...)

Catalog No. T23177 Copy Product Info
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PPACK Dihydrochloride is an efficient and selective irreversible thrombin inhibitor, which is often used in anticoagulant research, and can be used as a substitute anticoagulant for heparin lithium in blood gas and whole blood electrolyte analysis. PPACK is also used to regulate serine protease-related processes, which has application value in the study of thrombosis and fibrinolysis-related mechanisms.

PPACK Dihydrochloride

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Catalog No. T23177
Synonyms Pebac dihydrochloride, D-Phe-Pro-Arg-CH2Cl 2HCl, D-Phenylalanyl-prolyl-arginyl Chloromethyl Ketone dihydrochloride

PPACK Dihydrochloride is an efficient and selective irreversible thrombin inhibitor, which is often used in anticoagulant research, and can be used as a substitute anticoagulant for heparin lithium in blood gas and whole blood electrolyte analysis. PPACK is also used to regulate serine protease-related processes, which has application value in the study of thrombosis and fibrinolysis-related mechanisms.

PPACK Dihydrochloride
Cas No. 82188-90-7
Pack SizePriceUSA StockGlobal StockQuantity
5 mg$4683-6 months3-6 months
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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Color:White
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Product Introduction

Bioactivity
Description
PPACK Dihydrochloride is an efficient and selective irreversible thrombin inhibitor, which is often used in anticoagulant research, and can be used as a substitute anticoagulant for heparin lithium in blood gas and whole blood electrolyte analysis. PPACK is also used to regulate serine protease-related processes, which has application value in the study of thrombosis and fibrinolysis-related mechanisms.
In vitro
PPACK Dihydrochloride can effectively inhibit thrombin, and its Ki value is 3.7 × 10-8 M[2].
PPACK Dihydrochloride (0.2 mM; 2 h coincubation, 12 h measurement) can reduce the permeability increase induced by plasmin in the confluent bovine aortic endothelial cell monolayer by 59% at 12 hours after the initial exposure of plasmin, and completely inhibit the activity of plasmin [3].
PPACK Dihydrochloride (0.2 mM; 4 h post plasmin treatment can alleviate the morphological damage of confluent bovine aortic endothelial cells induced by plasmin, including reducing intercellular space and maintaining the stress fiber structure of F-actin, which was detected after 4 hours of initial plasmin treatment [3].
In vivo
PPACK Dihydrochloride (0.05-0.5 mg/kg; i.v.; Single bolus injection) plays a significant and dose-dependent antithrombotic role in the rat mesenteric microthrombosis model induced by He-Ne laser. Its minimum effective dose to arterioles and venules is 0.1 mg/kg, and it reaches its maximum activity immediately after a single intravenous injection, and the activity can be maintained for 60 minutes[2].
SynonymsPebac dihydrochloride, D-Phe-Pro-Arg-CH2Cl 2HCl, D-Phenylalanyl-prolyl-arginyl Chloromethyl Ketone dihydrochloride
Chemical Properties
Molecular Weight523.88
FormulaC21H33Cl3N6O3
Cas No.82188-90-7
SmilesN=C(N)NCCC[C@@H](C(CCl)=O)NC([C@H]1N(CCC1)C([C@H](N)CC2=CC=CC=C2)=O)=O.Cl.Cl
Relative Density.no data available
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: 100.00 mg/mL (190.88 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.9088 mL9.5442 mL19.0883 mL95.4417 mL
5 mM0.3818 mL1.9088 mL3.8177 mL19.0883 mL
10 mM0.1909 mL0.9544 mL1.9088 mL9.5442 mL
20 mM0.0954 mL0.4772 mL0.9544 mL4.7721 mL
50 mM0.0382 mL0.1909 mL0.3818 mL1.9088 mL
100 mM0.0191 mL0.0954 mL0.1909 mL0.9544 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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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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