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2138861-99-9

    1. 2138861-99-9 Structure

      2138861-99-9 Structure
      IdentificationBack Directory
      [Name]

      ABBV-744
      [CAS]

      2138861-99-9
      [Synonyms]

      CPD1639
      CS-2875
      ABBV-744
      ABBV-744; ABBV 744; ABBV744;2138861-99-9
      N-Ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-1H-pyrrolo[2,3-c]pyridine-2-carboxamide
      1H-Pyrrolo[2,3-c]pyridine-2-carboxamide, N-ethyl-4-[2-(4-fluoro-2,6-dimethylphenoxy)-5-(1-hydroxy-1-methylethyl)phenyl]-6,7-dihydro-6-methyl-7-oxo-
      [Molecular Formula]

      C28H30FN3O4
      [MDL Number]

      MFCD31657409
      [MOL File]

      2138861-99-9.mol
      [Molecular Weight]

      491.55
      Chemical PropertiesBack Directory
      [Boiling point ]

      663.7±55.0 °C(Predicted)
      [density ]

      1.262±0.06 g/cm3(Predicted)
      [storage temp. ]

      Store at -20°C
      [solubility ]

      DMSO:33.57(Max Conc. mg/mL);68.29(Max Conc. mM)
      DMSO:PBS (pH 7.2) (1:3):0.25(Max Conc. mg/mL);0.51(Max Conc. mM)
      DMF:30.0(Max Conc. mg/mL);61.03(Max Conc. mM)
      [form ]

      A crystalline solid
      [pka]

      13.77±0.40(Predicted)
      [color ]

      White to light yellow
      [InChIKey]

      OEDSFMUSNZDJFD-UHFFFAOYSA-N
      [SMILES]

      C1(=O)N(C)C=C(C2=CC(C(O)(C)C)=CC=C2OC2=C(C)C=C(F)C=C2C)C2C=C(C(NCC)=O)NC1=2
      Safety DataBack Directory
      [Symbol(GHS) ]

      Exclamation Mark (GHS07)
      GHS07
      [Signal word ]

      Warning
      Hazard InformationBack Directory
      [Uses]

      ABBV 744 is a bromodomain and extra-??terminal (BET) inhibitor used as a combination therapy for cancer treatment.
      [Biological Activity]

      ABBV-744 is a BDII-selective BET bromodomain inhibitor that inhibits BRD2, BRD3 and BRD4. It can be further studied for the treatment of acute myeloid leukemia and cancer.
      [in vitro]

      ABBV-744 is a potent BDII inhibitor that inhibits BRD2/3/4. The binding preference for BDII is more than 250 times that for BDI, with favorable drug-like properties. It is also an inhibitor of the androgen receptor transduction pathway.

      [in vivo]

      The maximum tolerated dose of ABBV-744 induces tumor growth inhibition in AML and prostate cancer xenograft models.

      [target]

      TargetValue
      BDII
      ()
      [IC 50]

      BRD2 (BD2): 8 nM (IC50); BRD3 (BD2): 13 nM (IC50); BRDT (BD2): 18 nM (IC50); BRD4 (BD2): 4 nM (IC50); BRD4 (BD2): 3 nM (Kd)
      Spectrum DetailBack Directory
      [Spectrum Detail]

      ABBV-744(2138861-99-9)1HNMR
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