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HIT220913490
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HIT220913490
  • HIT ID:HIT220913490
  • Cas No:1226801-23-5
  • 常用名:LY2780301
  • IUPAC:4-(4-{1-[2-(dimethylamino)ethyl]-4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}piperidin-1-yl)-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one
    IUPAC:4-(4-{1-[2-(dimethylamino)ethyl]-4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}piperidin-1-yl)-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one
  • InChI key:InChIKey=YDFKZIGAUIKZGP-UHFFFAOYSA-N
  • 分子式:C25H27F4N7O
  • 分子量:517.533
  • 氢键供体数 (HBD):
  • 氢键受体数 (HBA):
  • LogP:
  • SMILES:CN(C)CCn1cc(nc1C1CCN(CC1)c1ncnc2NC(=O)Cc12)-c1ccc(F)c(c1)C(F)(F)F
    SMILES:CN(C)CCn1cc(nc1C1CCN(CC1)c1ncnc2NC(=O)Cc12)-c1ccc(F)c(c1)C(F)(F)F
  • LY2780301 is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity. Akt inhibitor LY2780301 binds to and inhibits the activity of Akt, which may result in inhibition of the PI3K/Akt signaling pathway, thereby leading to inhibition of cell proliferation and the induction of apoptosis in tumor cells. Activation of the PI3K/Akt signaling pathway is frequently associated with tumorigenesis and dysregulated PI3K/Akt signaling may contribute to tumor resistance to a variety of antineoplastic agents.
市场产品/服务共显示1个结果
  • 供应商
    TargetMolSC
    规格
    货期
    8-10周
    纯度
    -
    ¥ 13,900.00
    1

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