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  • GSK2141795
GSK2141795的可视化放大

GSK2141795

A selective Akt inhibitor

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GSK2141795的二维码
  • 库存: 现货
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  • 5mg
    ¥1037.00
    830.00
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  • 50mg
    ¥5937.00
    4750.00
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  • 100mg
    ¥7775.00
    6220.00
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  • 200mg
    ¥13350.00
    10680.00
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  • 货号: ajci8852
  • CAS: 1047634-65-0
  • 别名: GSK2141795
  • 分子式: C18H16Cl2F2N4O2
  • 分子量: 429.25
  • 纯度: >98%
  • 溶解度: DMF: 1 mg/ml,DMSO: 1 mg/ml
  • 储存: Store at -20°C
  • 库存: 现货

Background

Uprosertib (GSK2141795) is a potent and selective pan-Akt inhibitor with IC50 values of 180/328/38 nM for Akt1/Akt2/Akt3, respectively.


Uprosertib (GSK2141795) inhibits Akt1/2/3 with the Kd values of 16/49/5 nM, respectively. Uprosertib potently inhibits only the PKC family members PRKACA and PRKACB as well as the cGMP-dependent protein kinase PRKG1 aqpart from the Akts. Protein targets that bind Uprosertib (GSK2141795) in the lysate show a dose-dependent reduction in binding to the kinobeads, while proteins unaffected by the drug show no reduction in binding[1].


参考文献:
[1]. Pachl F, et al. Characterization of a chemical affinity probe targeting Akt kinases. J Proteome Res. 2013 Aug 2;12(8):3792-800.
[2]. Jacobsen K, et al. Convergent Akt activation drives acquired EGFR inhibitor resistance in lung cancer. Nat Commun. 2017 Sep 4;8(1):410.

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