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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
BAY-4931 is a potent, covalent and selective PPARγ inverse-agonist with an IC 50 of 0.17 nM
In Vitro
BAY-4931 (0-10 μM; 7 days) inhibits UM-UC-9 proliferation with an IC 50 of 3.4 nM. BAY-4931 only inhibits CYP2C8 in CYP inhibition test. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Cell Proliferation AssayCell Line: UM-UC-9 cells Concentration: 0-10 μM Incubation Time: 7 days Result: Inhibited proliferation with an IC 50 of 3.4 nM.
Form:Solid
IC50& Target:PPAR-γ 0.17 nM (IC 50 , RT112-FABP4-NLucP cellular reporter assay) mouse PPARγ 0.14 nM (IC 50 , GAL4-NHR-LBD one hybrid reporter assay ) hPPARγ 0.40 nM (IC 50 , GAL4-NHR-LBD one hybrid reporter assay )
| 分子量 | 421.83 |
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Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| 溶解度 | DMSO : 125 mg/mL (296.33 mM; ultrasonic and warming and heat to 70°C) |
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