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  • Search results for: 'research area epigenetics parp'

Search results for: 'research area epigenetics parp'

Items 21-30 of 55

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  1. BMN 673
    A4153 BMN 673
    Summary: Potent PARP inhibitor
  2. AG-14361
    A4158 AG-14361
     1 Citation
    Summary: Potent PARP1 inhibitor
  3. Vorinostat (SAHA, MK0683)
    A4084 Vorinostat (SAHA, MK0683)
     9 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC inhibitor
      insoluble in EtOH; insoluble in H2O; ≥4.41 mg/mL
  4. Mocetinostat (MGCD0103, MG0103)
    A4089 Mocetinostat (MGCD0103, MG0103)
     2 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC inhibitor,isotype-selective and potent
      insoluble in EtOH; insoluble in H2O; ≥19.8 mg/mL
  5. Tubacin
    A4501 Tubacin
     3 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC6 inhibitor,potent,selective,reversible,cell-permeable
      insoluble in EtOH; insoluble in H2O; ≥7.19 mg/mL
  6. Resminostat (RAS2410)
    A4108 Resminostat (RAS2410)
     1 Citation
    Summary: Potent HDAC inhibitor
      Soluble in DMSO
  7. Pracinostat (SB939)
    A4095 Pracinostat (SB939)
     2 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: Pan-HDAC inhibitor
      insoluble in H2O; ≥11.4 mg/mL
  8. Belinostat (PXD101)
    A4096 Belinostat (PXD101)
     2 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: Hydroxamate-type HDAC inhibitor
      insoluble in H2O; ≥15.92 mg/mL
  9. Droxinostat
    A4100 Droxinostat
     2 Citation
    Summary: Selective HDAC inhibitor
  10. Tubastatin A
    A4101 Tubastatin A
     6 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC6 inhibitor,potent and selective
      insoluble in EtOH; insoluble in H2O; ≥10.75 mg/mL

Items 21-30 of 55

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