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BAY-0069 is a potent and selective PPARγ transactivator, inhibiting human PPARγ and murine PPARγ with IC50 values of 6.3 nM and 24 nM, respectively. BAY-0069 can be used in cancer research.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 5 mg | $34 | In Stock | In Stock | |
| 10 mg | $54 | In Stock | In Stock | |
| 25 mg | $121 | In Stock | In Stock | |
| 50 mg | $191 | In Stock | In Stock | |
| 100 mg | $289 | In Stock | In Stock | |
| 200 mg | $411 | - | In Stock |
| Description | BAY-0069 is a potent and selective PPARγ transactivator, inhibiting human PPARγ and murine PPARγ with IC50 values of 6.3 nM and 24 nM, respectively. BAY-0069 can be used in cancer research. |
| Targets&IC50 | PPARγ (human):6.3 nM, PPARγ (rat):24 nM, CYP2C8:4.3 μM |
| In vitro | BAY-0069 (0.0001, 0.001, 0.01, 0.01 and 1 μM; 7 days) leads to antiproliferative effects in the PPARγ-amplified cell line UM-UC-9.[1] |
| In vivo | BAY-0069 (1 μM; 1 h) exhibits superior microsomal stability, with a CL(b,hmic) of 0.47 L/h/kg in human liver microsomes and a CL(b,rhep) of 3.9 L/h/kg in rat liver hepatocytes.[1] |
| Molecular Weight | 466.28 |
| Formula | C22H16BrN3O4 |
| Cas No. | 420826-65-9 |
| Smiles | N(C(=O)C1=CC(N(=O)=O)=CC=C1Br)C=2C=C3C(OC(=N3)C4=CC=C(CC)C=C4)=CC2 |
| Relative Density. | 1.530 g/cm3 (Predicted) |
| Color | Yellow |
| Appearance | Solid |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 90 mg/mL (193.02 mM), Sonication and heating to 60℃ are recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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