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  • Search results for: 'research area cell cycle pten'

Search results for: 'research area cell cycle pten'

Items 61-70 of 76

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  1. Tofacitinib (CP-690550) Citrate
    A4135 Tofacitinib (CP-690550) Citrate
     2 Citation
    Target: JAK
    Summary: Potent JAK inhibitor
      ≥25.22 mg/mL
  2. Belinostat (PXD101)
    A4096 Belinostat (PXD101)
     2 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: Hydroxamate-type HDAC inhibitor
      insoluble in H2O; ≥15.92 mg/mL
  3. Cucurbitacin I
    A4512 Cucurbitacin I
    Target: STAT|JAK
    Summary: STAT3/JAK2 signaling inhibitor
      ≥22.45 mg/mL
  4. 4-HQN
    A4524 4-HQN
    Summary: PARP inhibitor
      ≥7.4 mg/mL
  5. MK-4827 hydrochloride
    B1163 MK-4827 hydrochloride
    Summary: PARP1/PARP2 inhibitor
      Soluble in DMSO
  6. MK-4827 tosylate
    B1164 MK-4827 tosylate
    Summary: PARP1/PARP2 inhibitor
      Soluble in DMSO
  7. 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
  8. ITF2357 (Givinostat)
    A4093 ITF2357 (Givinostat)
     2 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC inhibitor
      ≥23.8 mg/mL
  9. SGI-1776 free base
    A4192 SGI-1776 free base
     3 Citation
    Summary: Pim kinase inhibitor,ATP-competitive
      ≥40.5 mg/mL
  10. Tenovin-1
    A4203 Tenovin-1
    Target: Sir2-like Family Deacetylases (Sirtuins)|p53|p21
    Summary: SIRT2 inhibitor, activates p53
      insoluble in H2O; insoluble in EtOH; ≥15 mg/mL

Items 61-70 of 76

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