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  • Search results for: 'research area apoptosis bcl 2 family'

Search results for: 'research area apoptosis bcl 2 family'

Items 11-20 of 55

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  1. Teniposide
    A8532 Teniposide
    Summary: Topoisomerase inhibitor
      ≥23.65 mg/mL
  2. Adenine sulfate
    B1469 Adenine sulfate
    Summary: Sulfate salt form of adenine
      insoluble in EtOH; ≥66.9 mg/mL
  3. PCI-24781 (CRA-024781)
    A4098 PCI-24781 (CRA-024781)
    Target: Histone Deacetylases (HDACs)
    Summary: Pan-HDAC inhibitor
      insoluble in H2O; insoluble in EtOH; ≥11.75 mg/mL
  4. CI994 (Tacedinaline)
    A4102 CI994 (Tacedinaline)
     1 Citation
    Target: Histone Deacetylases (HDACs)
    Summary: HDAC inhibitor
      insoluble in H2O; insoluble in EtOH; ≥50 mg/mL
  5. ORY-1001
    B5882 ORY-1001
     1 Citation
    Summary: Selective inhibitor of KDM1A.
      insoluble in EtOH; ≥23.15 mg/mL
  6. CAY10603
    B4856 CAY10603
    Target: Histone Deacetylases (HDACs)
    Summary: potent and selective inhibitor of HDAC6
      ≥22.35 mg/mL
  7. Thiostrepton
    B7336 Thiostrepton
    Target: FoxM1
    Summary: Antibiotic that inhibits bacterial protein synthesis
      insoluble in EtOH; insoluble in H2O; ≥14.4 mg/mL
  8. Puromycin dihydrochloride
    B7587 Puromycin dihydrochloride
    Summary: allows selection for cells expressing the resistance gene puromycin N-acetyl-transferase (PAC) and successful Cas9-induced knock-in with puromycin resistance gene.
      ≥27.2 mg/mL
  9. Costunolide
    A3327 Costunolide
    Target: FPTase|Telomerases
    Summary: Apoptosis inducer
      ≥35.71 mg/mL
  10. MK-4827
    A3617 MK-4827
    Target: PARP
    Summary: PARP-1/-2 inhibitor,potent and selective
      ≥32 mg/mL

Items 11-20 of 55

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