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  • IKKε-IN-1
IKKε-IN-1的可视化放大

IKKε-IN-1

potent IKKε inhibitor

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IKKε-IN-1的二维码
  • 库存: 现货
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  • 5mg
    ¥2762.00
    2210.00
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  • 10mg
    ¥3925.00
    3140.00
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  • 50mg
    ¥12900.00
    10320.00
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  • 100mg
    ¥16200.00
    12960.00
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  • 货号: ajci10798
  • CAS: 1292310-49-6
  • 别名:
  • 分子式: C26H27N5O3
  • 分子量: 457.52
  • 纯度: >98%
  • 溶解度: Soluble in DMSO
  • 储存: Store at -20°C
  • 库存: 现货

Background

TBK1/IKKε-IN-2 is a dual TBK1 and IKKε inhibitor.


TBK1/IKKε-IN-2 (Cmpound #1) inhibits TBK1 biochemical function in Ulight kinase assay at 5 and 250 μM ATP concentration with IC50s of 0.6 and 2.6 nM, rsespectively. TBK1/IKKε-IN-2 inhibits IKKε biochemical function in Ulight kinase assay at 10 μM ATP with an IC50 of 3.9 nM. The IC50 of TBK1/IKKε-IN-2 in the Panc 02.13 proliferation assay is 5 μM[1].


参考文献:
[1]. Muvaffak A, et al. Evaluating TBK1 as a therapeutic target in cancers with activated IRF3. Mol Cancer Res. 2014 Jul;12(7):1055-66.

Protocol

Cell experiment:

Cell proliferation experiments are carried out in a 96-well format (6 replicates), Panc 02.13 cells are plated at a density of 2,000 to 5,000 cells per well. At 24 hours following cell seeding, the cells are treated with the tool inhibitor titrations (e.g., TBK1/IKKε-IN-2, 1 nM, 10 nM, 100 nM, 1 μM and 10 μM) for 4 days at 37°C and then assayed by using the ATP CellTiter-Glo luminescent cell viability assay[1].

参考文献:

[1]. Muvaffak A, et al. Evaluating TBK1 as a therapeutic target in cancers with activated IRF3. Mol Cancer Res. 2014 Jul;12(7):1055-66.

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