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  • Search results for: 'research area cell cycle rad51'

Search results for: 'research area cell cycle rad51'

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  1. PF-543
    A3717 PF-543
     1 Citation
    Target: Sphingosine kinases (SphKs)
    Summary: SphK1 inhibitor,cell-permeate,potent and selective
      ≥23.3 mg/mL
  2. BMS 182874 hydrochloride
    B5113 BMS 182874 hydrochloride
    Summary: ETA antagonist
      Soluble to 100 mM in DMSO
  3. DY131
    A3375 DY131
    Summary: ERRγ agonist
      insoluble in H2O; ≥37.1 mg/mL
  4. Methylprednisolone
    A4233 Methylprednisolone
    Target: Glucocorticoid Receptors
    Summary: Apoptosis inducer,GR agonist
      insoluble in H2O; ≥15.35 mg/mL
  5. BIM 23042
    B5401 BIM 23042
    Summary: Antagonist of neuromedin B receptor,selective
      ≥43.8 mg/mL
  6. Tranilast
    A5375 Tranilast
    Summary: Angiogenesis inhibitor
      ≥32.7 mg/mL
  7. APC 366 (trifluoroacetate salt)
    B7087 APC 366 (trifluoroacetate salt)
    Summary: mast cell tryptase inhibitor,selective and competitive
      Soluble to 5 mg/mL
  8. Parstatin (human)
    B5450 Parstatin (human)
    Summary: Cell-permeable peptide that inhibits angiogenesis and exhibits cardioprotective activity
      Soluble to 1 mg/mL
  9. Parstatin (mouse)
    B5451 Parstatin (mouse)
    Summary: Cell-permeable peptide that inhibits angiogenesis and exhibits cardioprotective activity
      Soluble to 1 mg/mL
  10. Montelukast Sodium
    B1792 Montelukast Sodium
    Summary: Leukotriene receptor antagonist
      ≥28.7 mg/mL

Items 1-10 of 21

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