Information BAY-985 is a potent and highly selectiveTBK1/IKKεinhibitor. BAY-985 shows high potency towardTBK1(IC50 = 2 nM, low ATP assay; 30 nM, high ATP assay) andIKKε(IC50 = 2 nM), as well as high potency in the mechanistic pIRF3 assay (IC50 = 74 nM), and an antiproliferative effect on SK-MEL-2 cells (IC50 = 900 nM). Targets TBK1 (in low ATP assay); IKKε (Cell-free assay); TBK1 (in high ATP assay); pIRF3 (Cell-free assay) 2 nM ;2 nM; 30 nM; 74 nM In vitro BAY-985 is a potent and highly selective TBK1/IKKε inhibitor that inhibits the cellular phosphorylation of interferon regulatory factor 3 and displays antiproliferative efficacy in the melanoma cell line SK-MEL-2. In vivo BAY-985 shows only weak antitumor activity in the SK-MEL-2 human melanoma xenograft model. Cell Research(from reference) Cell lines:ACHN, SK-MEL-2, MDA-MB231 cells Concentrations:100 nM Incubation Time:96 h
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BAY-985
CAS number:2409479-29-2 molecular formula:C27H30F3N9O
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| Chinese alias | - | ||
| English alias | 1-Propanone,1-[4-[(1R)-1-[2-[[6-[6-(dimethylamino)-4-pyrimidinyl]-1H-benzimidazol-2-yl]amino]-4-pyridinyl]ethyl]-1-piperazinyl]-3,3,3-trifluoro- | ||
| CAS number | 2409479-29-2 | molecular formula | C27H30F3N9O |
| molecular weight | 553.58 g/mol | Exact mass | - |
| PSA | 106.000 Ų | logp | 3.600 |
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