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BAY-0069

Catalog No. T67936Cas No. 420826-65-9

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.

BAY-0069

BAY-0069

Purity: 99.41%
Catalog No. T67936Cas No. 420826-65-9
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 SizePriceAvailabilityQuantity
1 mg$34In Stock
5 mg$80In Stock
10 mg$128In Stock
25 mg$289In Stock
50 mg$455In Stock
100 mg$690In Stock
500 mg$1,450In Stock
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Purity:99.41%
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Product Introduction

Bioactivity
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, CYP2C8:4.3 μM, PPARγ (rat):24 nM
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]
Chemical Properties
Molecular Weight466.28
FormulaC22H16BrN3O4
Cas No.420826-65-9
Storage & Solubility Information
StorageShipping with blue ice.
Solubility Information
DMSO: 90.0 mg/mL (193.0 mM), Sonication and heating to 60℃ are recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1446 mL10.7232 mL21.4463 mL107.2317 mL
5 mM0.4289 mL2.1446 mL4.2893 mL21.4463 mL
10 mM0.2145 mL1.0723 mL2.1446 mL10.7232 mL
20 mM0.1072 mL0.5362 mL1.0723 mL5.3616 mL
50 mM0.0429 mL0.2145 mL0.4289 mL2.1446 mL
100 mM0.0214 mL0.1072 mL0.2145 mL1.0723 mL

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