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MK-0533

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Catalog No. T68000LCas No. 668455-28-5

MK-0533 is a novel PPARγ partial agonist for the prevention of vascular endothelial dysfunction (VED) and VED-related cardiovascular disease.

MK-0533

MK-0533

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🥰Excellent
Purity: 99.99%
Catalog No. T68000LCas No. 668455-28-5
MK-0533 is a novel PPARγ partial agonist for the prevention of vascular endothelial dysfunction (VED) and VED-related cardiovascular disease.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$94In StockIn Stock
5 mg$231In StockIn Stock
10 mg$343In StockIn Stock
25 mg$551In StockIn Stock
50 mg$793In StockIn Stock
100 mg$1,090In StockIn 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.
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Batch Information

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Purity:99.99%
ee:97.88%
Appearance:Solid
Color:Yellow
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Product Introduction

MK-0533 AI Summary
MK-0533 is a potent agonist of human PPARgamma with an EC50 value of 2.0 nM. It also demonstrates agonist activity at human PPARalpha and PPARgamma in various cell lines, as well as in mouse, hamster, and dog PPARalpha. The compound displays high selectivity for PPARgamma over PPARalpha across different species. In db/db mice, it exhibits antihyperglycemic activity and modulates plasma adiponectin levels. Pharmacokinetic studies in rats, dogs, and monkeys reveal favorable bioavailability, clearance, and distribution profiles. Toxicological evaluations highlight potential effects on liver weight and adverse impacts on brown adipose tissue weight in Sprague-Dawley rats..
Note: Summary generated by AI. Data source: ChEMBL
Bioactivity
Description
MK-0533 is a novel PPARγ partial agonist for the prevention of vascular endothelial dysfunction (VED) and VED-related cardiovascular disease.
Chemical Properties
Molecular Weight527.49
FormulaC28H24F3NO6
Cas No.668455-28-5
SmilesCC=1N(C=2C(C1C(=O)C3=CC=C(OC)C=C3)=CC=C(OC(F)(F)F)C2)C4=CC(O[C@@H](C(O)=O)CC)=CC=C4
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: 55 mg/mL (104.27 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8958 mL9.4789 mL18.9577 mL94.7885 mL
5 mM0.3792 mL1.8958 mL3.7915 mL18.9577 mL
10 mM0.1896 mL0.9479 mL1.8958 mL9.4789 mL
20 mM0.0948 mL0.4739 mL0.9479 mL4.7394 mL
50 mM0.0379 mL0.1896 mL0.3792 mL1.8958 mL
100 mM0.0190 mL0.0948 mL0.1896 mL0.9479 mL

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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

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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