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Elinogrel potassium (Synonyms: PRT060128 potassium)

Catalog No. T88354 Copy Product Info
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Elinogrel (PRT060128) potassium functions as a reversible, competitive, and orally active antagonist of the P2Y12 receptor. This compound effectively inhibits thrombosis .

Elinogrel potassium

Copy Product Info
🥰Excellent
Catalog No. T88354
Synonyms PRT060128 potassium

Elinogrel (PRT060128) potassium functions as a reversible, competitive, and orally active antagonist of the P2Y12 receptor. This compound effectively inhibits thrombosis .

Elinogrel potassium
Cas No. 936501-01-8
Pack SizePriceUSA StockGlobal StockQuantity
25 mg$1,6708-10 weeks8-10 weeks
50 mg$2,1808-10 weeks8-10 weeks
100 mg$2,8008-10 weeks8-10 weeks
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
Elinogrel (PRT060128) potassium functions as a reversible, competitive, and orally active antagonist of the P2Y12 receptor. This compound effectively inhibits thrombosis .
In vivo
Elinogrel, administered orally at 60 mg/kg daily for three days, has been shown to inhibit thrombosis [2]. At a dose of 1 mg/kg intravenously, Elinogrel can prevent residual thrombosis in mice treated with clopidogrel at 50 mg/kg orally for three days in a FeCl3-induced vascular injury model [2]. Animal Model: C57BL/6J mice [2] Dosage: 60 mg/kg Administration: P.o.; daily for 3 days Result: Inhibited thrombosis in mouse.
SynonymsPRT060128 potassium
Chemical Properties
Molecular Weight562.03
FormulaC20H14ClFKN5O5S2
Cas No.936501-01-8
SmilesO=C([N-]S(=O)(C1=CC=C(Cl)S1)=O)NC2=CC=C(N3C(NC4=CC(NC)=C(C=C4C3=O)F)=O)C=C2.[K+]
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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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:
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:
mg/kg
g
μL
2 Enter the in vivo formulation:
% DMSO
%
% Tween 80
% Saline/PBS/ddH2O

Dose Conversion

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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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