Molecular Formula | C30H29N3O4 |
Molar Mass | 495.57 |
Density | 1.264±0.06 g/cm3(Predicted) |
Boling Point | 749.2±60.0 °C(Predicted) |
Solubility | DMSO: 20mg/mL |
Appearance | solid |
Color | yellow |
pKa | 3.91±0.10(Predicted) |
Storage Condition | Desiccate at +4°C |
In vitro study | GW1929 is a potent PPAR-γ activator, with pK i s of 8.84, < 5.5, and < 6.5 for human PPAR-γ, PPAR-α, and PPAR-δ, and pEC 50 s of 8.56 and 8.27 for human PPAR-γ and murine PPAR-γ, respectively. GW1929 (10 μM) inhibits TBBPA-induced caspase-3 increase and TBBPA-stimulated LDH release in neocortical cell cultures. |
In vivo study | GW1929 (0.5, 1, 5 mg/kg, p.o.) highly decreases nonfasted plasma glucose levels in Zucker diabetic fatty (ZDF) rats after treatment for 14 days, and possesses antilipolytic efficacy. GW1929 (1, 5 mg/kg, p.o.) increases glucose-stimulated insuline secretion of β-cell in ZDF rats. |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.018 ml | 10.089 ml | 20.179 ml |
5 mM | 0.404 ml | 2.018 ml | 4.036 ml |
10 mM | 0.202 ml | 1.009 ml | 2.018 ml |
5 mM | 0.04 ml | 0.202 ml | 0.404 ml |
biological activity | GW1929 is an effective PPAR-γ agonist, and the pKi of human PPAR-γ is 8.84. The pEC50 for human and mouse is 8.56 and 8.27 respectively. |
target | PPAR-γ 8.56 (pEC 50 , Human PPAR-γ) |
in vitro research | GW1929 is a potent PPAR-γ activator, with pK I s of 8.84, < 5.5, and < 6.5 for human PPAR-γ, PPAR-α, and PPAR-δ, and pEC 50 s of 8.56 and 8.27 for human PPAR-γ and murine PPAR-γ, respectively. GW1929 (10 μM) inhibits TBBPA-induced caspase-3 increase and TBBPA-stimulated LDH release in neocortical cell cultures. |
in vivo study | GW1929 (0.5, 1, 5 mg/kg, p.o.) high decreases nonfasted plasma glucose levels in Zucker diabetic fatty (ZDF) rats after treatment for 14 days, and possesses antilipolytic efficacy. GW1929 (1, 5 mg/kg, P. o.) increases glucose-stimulated insuline secretion of β-cell in ZDF rats. |