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Thiamine pyrophosphate tetrahydrate

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Catalog No. TYD-04496

Thiamine pyrophosphate tetrahydrate is the coenzyme form of vitamin B1 and acts as a crucial intermediate in the pyruvate dehydrogenase complex and alpha-ketoglutarate dehydrogenase complex. It functions as a cofactor for α-keto acid dehydrogenases, which are essential for oxidative phosphorylation and the pentose phosphate pathway.

Thiamine pyrophosphate tetrahydrate

Thiamine pyrophosphate tetrahydrate

Copy Product Info
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Catalog No. TYD-04496
Thiamine pyrophosphate tetrahydrate is the coenzyme form of vitamin B1 and acts as a crucial intermediate in the pyruvate dehydrogenase complex and alpha-ketoglutarate dehydrogenase complex. It functions as a cofactor for α-keto acid dehydrogenases, which are essential for oxidative phosphorylation and the pentose phosphate pathway.
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Product Introduction

Bioactivity
Description
Thiamine pyrophosphate tetrahydrate is the coenzyme form of vitamin B1 and acts as a crucial intermediate in the pyruvate dehydrogenase complex and alpha-ketoglutarate dehydrogenase complex. It functions as a cofactor for α-keto acid dehydrogenases, which are essential for oxidative phosphorylation and the pentose phosphate pathway.
In vivo
Thiamine pyrophosphate (25 mg/kg, intraperitoneal injection) tetrahydrate inhibits oxidative damage induced by ischemia-reperfusion in rat ovarian tissue. Additionally, thiamine pyrophosphate (20 mg/kg, intraperitoneal injection, once daily for 14 days) tetrahydrate prevents cisplatin-induced cardiotoxicity in rats, as well as the associated oxidative stress and cardiac injury.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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

Dose Conversion

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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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