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PPARα/γ agonist 4

PPARα/γ agonist 4
Compound (S)-7, also known as PPARα/γ agonist 4, is a dual potent agonist for PPARα and PPARγ with EC50 values of 0.061 μM and 1.42 μM, respectively. This compound exhibits oral efficacy and operates through an insulin-independent mechanism, featuring mitochondrial pyruvate carrier inhibition and antidiabetic properties. PPARα/γ agonist 4 holds potential for research in dyslipidemic type 2 diabetes.
Catalog No. T89021

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PPARα/γ agonist 4

Catalog No. T89021

Compound (S)-7, also known as PPARα/γ agonist 4, is a dual potent agonist for PPARα and PPARγ with EC50 values of 0.061 μM and 1.42 μM, respectively. This compound exhibits oral efficacy and operates through an insulin-independent mechanism, featuring mitochondrial pyruvate carrier inhibition and antidiabetic properties. PPARα/γ agonist 4 holds potential for research in dyslipidemic type 2 diabetes.
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Product Introduction

Bioactivity
Description
Compound (S)-7, also known as PPARα/γ agonist 4, is a dual potent agonist for PPARα and PPARγ with EC50 values of 0.061 μM and 1.42 μM, respectively. This compound exhibits oral efficacy and operates through an insulin-independent mechanism, featuring mitochondrial pyruvate carrier inhibition and antidiabetic properties. PPARα/γ agonist 4 holds potential for research in dyslipidemic type 2 diabetes.
In vitro
PPARα/γ agonist 4 (100 nM, 24 hours) enhances glucose uptake and metabolism in the C2C12 cell line and prevents lipid accumulation in liver or muscle cells by boosting mitochondrial activity associated with fatty acid degradation.
In vivo
Compound PPARα/γ agonist 4, administered orally at doses of 25 mg/kg and 50 mg/kg over a 15-day treatment period, exhibits dose-dependent antihyperglycemic effects and significant lipid-lowering properties in a diabetic mouse model.
Chemical Properties
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

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