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BAY-985

BAY-985
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Purity:99.3%
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BAY-985

Catalog No. T10477Cas No. 2409479-29-2
BAY-985 is a potent, selective, and orally active ATP-competitive dual inhibitor of TBK1 and IKKε (IC50s: 2/30 and 2 nM for TBK1 (low/high ATP) and IKKε) with antitumor efficacy.
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Pack SizePriceAvailabilityQuantity
1 mg$175In Stock
5 mg$372In Stock
10 mg$597In Stock
25 mg$953In Stock
50 mg$1,290In Stock
100 mg$1,730In Stock
1 mL x 10 mM (in DMSO)$453In Stock
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Product Introduction

Bioactivity
Description
BAY-985 is a potent, selective, and orally active ATP-competitive dual inhibitor of TBK1 and IKKε (IC50s: 2/30 and 2 nM for TBK1 (low/high ATP) and IKKε) with antitumor efficacy.
In vitro
BAY-985 inhibits FLT3, RSK4, DRAK1, and ULK1 (IC50s: 123, 276, 311, and 7930 nM). BAY-985 inhibits the cellular phosphorylation of interferon regulatory factor 3 (IRF3, IC50: 74 nM). BAY-985 shows anti-proliferative activity in a few cancer cell lines (IC50s: 900 and 7260 nM for SK-MEL2 (NRAS and TP53 mutated) and ACHN (CDKN2A mutated) cells).
In vivo
BAY-985 (200 mg/kg; p.o.; b.i.d.; 111 days) results in weak antitumor efficacy. BAY-985 shows high clearance (CLb= 4.0 L/h/kg, ca. 95% hepatic extraction), large volume of distribution at steady state (Vss=2.9 L/kg) and a short terminal half-life (t1/2=0.79 h).
Chemical Properties
Molecular Weight553.58
FormulaC27H30F3N9O
Cas No.2409479-29-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 50 mg/mL (90.32 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.8064 mL9.0321 mL18.0642 mL90.3212 mL
5 mM0.3613 mL1.8064 mL3.6128 mL18.0642 mL
10 mM0.1806 mL0.9032 mL1.8064 mL9.0321 mL
20 mM0.0903 mL0.4516 mL0.9032 mL4.5161 mL
50 mM0.0361 mL0.1806 mL0.3613 mL1.8064 mL

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