AT-7867

AT-7867

参考价:¥2211
供货周期: 一周
品牌: 爱必信
规格: 98% min
货号: abs812007
CAS号: 857531-00-1
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抑制剂描述:

产品名称:AT-7867

产品别名:见爱必信官网

英文别名:AT-7867

靶点:Akt

CAS:857531-00-1

纯度:98% min

外观:见爱必信官网

保存方法:store at -20℃ for one year(Powder); in DMSO or others solvent store at 2-4℃ for two weeks, at -20℃ for six months.

描述:

AT-7867是一种有效的,ATP竞争性的Akt1/2/3和p70S6K/PKA抑制剂,无细胞试验中IC50分别为32 nM/17 n/47 nM和85 nM/20 nM,对AGC激酶家族以外几乎没有抑制活性。

溶解性:DMSO 68 mg/mL (201.27 mM)
Ethanol 5 mg/mL (14.79 mM)
Water Insoluble

体外研究:

AT7867 also inhibits structurally related AGC kinases p70S6K and PKA with IC50 of 20 nM and 85 nM, respectively. AT7867 shows ATP-competitive activity to Akt2 with Ki of 18 nM. AT7867 exhibits antiproliferation in cell lines with PTEN or PIK3CA mutations and shows great potent to MES-SA, MDA-MB-468, MCF-7, HCT116 and HT29 with IC50 of 0.94 μM, 2.26 μM, 1.86 μM, 1.76 μM and 3.04 μM, respectively. AT7867 also suppresses the cell growth of U87MG, PC-3 and DU145 cells with IC50 of 8.22 μM, 10.37 μM and 11.86 μM, respectively. AT7867 suppresses Akt activity by inhibiting phosphorylation of GSK-3β in human tumor cells with IC50 of 2-4 μM. AT7867 also induces the phosphorylation of the following Akt direct substrates including proapoptotic transcription factors FKHR (FoxO1a), FKHRL1 (FoxO3a) and the downstream target S6RP in U87MG cells.

体内研究:AT7867 shows bioavailability of 44% in mice by p.o. route. AT7867 could increase the cleaved PARP in MES-SA xenografts at 20 mg/kg i.p. or 90 mg/kg p.o.. AT7867 significantly inhibits the tumor growth in MES-SA xenografts or U87MG xenografts with T/C of 0.37 and 0.51, respectively.

产品信息订购:

  产品货号   产品名称   规格 价格 大包装及货期
  abs812007   AT-7867   10mg   2211.00   立即咨询
  abs812007   AT-7867   50mg   6680.00   立即咨询

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