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S87108

AKTI-2008

源叶(MedMol) 99%
  • 英文名:
  • AKTI-2008
  • 别名:
  • CAS号:
  • 893422-47-4
  • 分子式:
  • C33H29N7O
  • 分子量:
  • 539.64
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源叶(MedMol) S87108-5mg 99% ¥3500.00元 预计交期:2-3天 - - - EA 加入购物车
源叶(MedMol) S87108-10mg 99% ¥5000.00元 预计交期:2-3天 - - - EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: Akt1/Akt2-IN-1 (Compound 17) is an allosteric inhibitor of Akt1 (IC50=3.5 nM) and Akt2 (IC50=42 nM), with potent and balanced activity
  • 靶点: Akt1:3.5 nM (IC50);Akt2:42 nM (IC50);Akt
  • 体内研究:
    Akt1/Akt2-IN-1 (Compound 17) is well tolerated in at exposures that provide high levels of Akt1 and 2 inhibition in vivo. Akt1/Akt2-IN-1 has also been shown to inhibit the growth of A2780 tumors in vivo when used as monotherapy. Akt1/Akt2-IN-1 has potent inhibitory activity against Akt1 and 2 in vivo in a mouse lung and efficacy in a tumor xenograft model. Akt1/Akt2-IN-1 shows good pharmacokinetics in rat with a low clearance of 4.6 mL/min/kg and a half-life of 3.8 h. Due to the improved cell potency, physical properties, and rodent pharmacokinetics of Akt1/Akt2-IN-1, tolerability and Akt inhibition are assessed in mice. Using an acute dosing schedule (IP dosing of 50 mg/kg at times 0, 3, and 8 h), administration of Akt1/Akt2-IN-1 is well tolerated in mice and shows high levels of Akt inhibition in mouse lung
  • 参考文献:
    1. Bilodeau MT, Allosteric inhibitors of Akt1 and Akt2: a naphthyridinone with efficacy in an A2780 tumor xenograft model. Bioorg Med Chem Lett. 2008 Jun 1;18(11):3178-82.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: 2-8℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 1.853 ml 9.265 ml 18.531 ml
    5 mM 0.371 ml 1.853 ml 3.706 ml
    10 mM 0.185 ml 0.927 ml 1.853 ml
    50 mM 0.037 ml 0.185 ml 0.371 ml
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