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HIT212672592
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HIT212672592
  • HIT ID:HIT212672592
  • Cas No:1456858-57-3
  • 常用名:MRT199665
  • IUPAC:7-[(1S)-4-hydroxy-2,3-dihydro-1H-inden-1-yl]-5,5-dimethyl-2-({3-[(pyrrolidin-1-yl)methyl]phenyl}amino)-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one
    IUPAC:7-[(1S)-4-hydroxy-2,3-dihydro-1H-inden-1-yl]-5,5-dimethyl-2-({3-[(pyrrolidin-1-yl)methyl]phenyl}amino)-5H,6H,7H-pyrrolo[2,3-d]pyrimidin-6-one
  • InChI key:OFIFLUFVENTCNZ-QHCPKHFHSA-N
  • 分子式:C28H31N5O2
  • 分子量:469.589
  • 氢键供体数 (HBD):2
  • 氢键受体数 (HBA):6
  • LogP:4.552842
  • SMILES:CC1(C)C(=O)N([C@H]2CCc3c2cccc3O)c2nc(Nc3cccc(CN4CCCC4)c3)ncc12
    SMILES:CC1(C)C(=O)N([C@H]2CCc3c2cccc3O)c2nc(Nc3cccc(CN4CCCC4)c3)ncc12
  • MRT199665 is an effective and ATP-competitive, selective MARK/SIK/AMPK inhibitor (IC50s of 2/2/3/2 nM, 10/10 nM, and 110/12/43 nM for MARK1/MARK2/MARK3/MARK14, AMPKα1/AMPKα2, and SIK1/SIK2/SIK3, respectively). MRT199665 suppresses the phosphorylation of SIK substrate CRTC3 at S370. MRT199665 induces apoptosis in MEF2C-activated human acute myeloid leukemia (AML) cells.
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  • 供应商
    TargetMolSC
    规格
    货期
    8-10周
    纯度
    -
    待询
    1

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