MD001
Modify Date: 2024-01-06 22:19:31
MD001 structure
|
Common Name | MD001 | ||
|---|---|---|---|---|
| CAS Number | 2254605-76-8 | Molecular Weight | 398.407 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 575.1±45.0 °C at 760 mmHg | |
| Molecular Formula | C25H18O5 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | 199.1±22.2 °C | |
Use of MD001MD001 is a dual agonist of peroxisome proliferator-activated receptor α (PPARα) and PPARγ. It binds to PPARα and PPARγ but does not bind to PPARβ/δ. It increases transcriptional activity of PPARα and PPARγ and glucose consumption. MD001 decreases levels of glucose, insulin, free fatty acids, triglycerides, LDL, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) in blood and reduces the size and number of hepatic lipid droplets in diabetic db/db mice. |
| Name | MD001 |
|---|---|
| Synonym | More Synonyms |
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 575.1±45.0 °C at 760 mmHg |
| Molecular Formula | C25H18O5 |
| Molecular Weight | 398.407 |
| Flash Point | 199.1±22.2 °C |
| Exact Mass | 398.115417 |
| LogP | 6.14 |
| Vapour Pressure | 0.0±1.6 mmHg at 25°C |
| Index of Refraction | 1.704 |
| 2H-1-Benzopyran-2-one, 5,7-dihydroxy-8-methyl-3-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-4-phenyl- |
| MD001 |
| 5,7-Dihydroxy-8-methyl-4-phenyl-3-[(2E)-3-phenyl-2-propenoyl]-2H-chromen-2-one |