| Name | 5-[[4-[2-(5-methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1-benzothiophen-7-yl]methyl]-1,3-thiazolidine-2,4-dione | 
|---|---|
| Synonyms | 
                                
                                UNII:8GKF7V499B
                                
                                
                                 EX-8519 5-({4-[2-(5-Methyl-2-phenyl-1,3-oxazol-4-yl)ethoxy]-1-benzothiophen-7-yl}methyl)-1,3-thiazolidine-2,4-dione UNII-8GKF7V499B Edaglitazone 2,4-Thiazolidinedione, 5-[[4-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]benzo[b]thien-7-yl]methyl]- 5-((4-(2-(5-methyl-2-phenyloxazol-4-yl)ethoxy)benzo[b]thiophen-7-yl)methyl)thiazolidine-2,4-dione  | 
                        
| Description | Edaglitazone is a potent, selective and orally active PPARγ agonist, with EC50s of 35.6 nM and 1053 nM for PPARα and PPARγ, respectively. Edaglitazone displays antiplatelet, antidiabetic and anti-hyperglycemic activity[1][2][3]. | 
|---|---|
| Related Catalog | |
| Target | 
                                
                                 PPARγ:35.6 nM (EC50) PPARα:1053 nM (EC50)  | 
                        
| In Vitro | Edaglitazone (3-16 μM; 5 min) inhibits the collagen (1.2 μg/mL)-induced platelet aggregation. Edaglitazone increases the intraplatelet levels of cAMP in a concentration dependent manner. Edaglitazone preventes the Collagen-induced intraplatelet levels of PPARγ decrease[3]. | 
| In Vivo | Edaglitazone (4.4 mg/kg; p.o. daily for 10 days) enhances insulin sensitivity in obese rats[2]. | 
| References | 
| Density | 1.4±0.1 g/cm3 | 
|---|---|
| Molecular Formula | C24H20N2O4S2 | 
| Molecular Weight | 464.56 | 
| Exact Mass | 464.086456 | 
| PSA | 138.46000 | 
| LogP | 6.20 | 
| Index of Refraction | 1.673 |