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AZD8055(≥99%)北京现货

产品信息
  • 特别提示:包括AZD8055在内,本公司的所有产品仅可用于科研实验,严禁用于临床YL及其他非科研用途!


    产品名称:AZD8055
    英文名称:AZD8055
    产品货号:L10089
    产品规格:10mg|50mg
     属性
    CAS号 1009298-09-2
    分子式 C25H31N5O4
    分子量 465.56
    溶解性 DMSO ≥90mg/mL Water ≥1.8mg/mL Ethanol ≥13mg/mL
    存贮条件 储存温度-20℃
    密度 1.2480
    描述
    产品介绍 AZD8055是ATP竞争性mTORYZ剂,IC50为0.8 nM,比对PI3K和ATM/DNA-PK的YZ性强超过1000倍。
    备注 AZD8055 is a novel ATP-competitivemTORinhibitor withIC50of 0.8 nM with excellent selectivity(?1,000-fold) against PI3K isoforms and ATM/DNA-PK.Phase 1.
    生化机理 AZD8055 shows low activity(~1,000-fold) against all PI3K isoforms(α,β,γ,δ) and other members of the PI3K-like kinase family(ATM and DNA-PK).AZD8055 inhibits the phosphorylation of mTORC1(p70S6K and 4E-BP1) as well as phosphorylation of the mTORC2(Akt) and downstream proteins.The rapamycin-resistant T37/46 phosphorylation sites on 4E-BP1 can be fully inhibited by AZD8055,resulting in significant inhibition of cap-dependent translation.AZD8055 potently inhibits proliferation in U87MG,A549 and H838 cells with IC50 of 53,50 and 20 nM,respectively.AZD8055 also induces autophagy and increased LC3-II levels in H838 and A549 cells[1].AZD8055 decreases AML blast cell proliferation and cell cycle progression,reduces the clonogenic growth of leukemic progenitors and induces caspase-dependent apoptosis in leukemic cells but not in normal immature CD34+ cells
    别名 (5-(2,4-二((3S)-3-甲基mǎ啉-4-基)bǐ啶并(2,3-d)嘧啶-7-基)-2-jiǎ氧基苯基)jiǎ醇;;AZD8055;AZD 8055;(5-(2,4-bis((3s)-3-methylmorpholin-4-yl)pyrido(2,3-d)pyrimidin-7-yl)-2-methoxyphenyl)methanol
    温馨提示:不可用于临床ZL。
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