BAY-985

BAY-985

CAT N°: 34234
Price:

From 122.00 103.70

BAY-985 is a dual inhibitor of TANK-binding kinase 1 (TBK1) and I?B kinase ? (IKK?; IC50 = 2 nM for both).{58566} It is selective for TBK1 and IKK? over FLT3, RSK4, DRAK1, and ULK1 (IC50s = 123, 276, 311, and 7,390 nM, respectively). BAY-985 inhibits phosphorylation of interferon regulatory factor 3 (IRF3) in MDA-MB-231 cells expressing mouse IRF3 (IC50 = 74 nM). It inhibits the proliferation of SK-MEL-2 cells in vitro (IC50 = 900 nM) and reduces tumor weight in an SK-MEL-2 mouse xenograft model when administered at a dose of 200 mg/kg.

Territorial Availability: Available through Bertin Technologies only in France

  • Synonyms
    • 1-[4-[(1R)-1-[2-[[6-[6-(dimethylamino)-4-pyrimidinyl]-1H-benzimidazol-2-yl]amino]-4-pyridinyl]ethyl]-1-piperazinyl]-3,3,3-trifluoro-1-propanone
  • Correlated keywords
    • BAY985 TBK 1 IKK ? FLT 3 RSK 4 DRAK ULK MDAMB231 SKMEL2
  • Product Overview:
    BAY-985 is a dual inhibitor of TANK-binding kinase 1 (TBK1) and I?B kinase ? (IKK?; IC50 = 2 nM for both).{58566} It is selective for TBK1 and IKK? over FLT3, RSK4, DRAK1, and ULK1 (IC50s = 123, 276, 311, and 7,390 nM, respectively). BAY-985 inhibits phosphorylation of interferon regulatory factor 3 (IRF3) in MDA-MB-231 cells expressing mouse IRF3 (IC50 = 74 nM). It inhibits the proliferation of SK-MEL-2 cells in vitro (IC50 = 900 nM) and reduces tumor weight in an SK-MEL-2 mouse xenograft model when administered at a dose of 200 mg/kg.

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