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  • Search results for: 'research area pi3k akt signaling pi3k inhibitors'

Search results for: 'research area pi3k akt signaling pi3k inhibitors'

Items 1-10 of 18

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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. SCH 527123
    A3802 SCH 527123
     5 Citation
    Target: CXCR
    Summary: CXCR1 and CXCR2 receptors antagonist
  3. Perindopril
    B1214 Perindopril
    Target: Angiotensin-Converting Enzymes (ACEs)
    Summary: ACE inhibitor
      Soluble in DMSO
  4. 5-Iodotubercidin
    A3125 5-Iodotubercidin
    Target: Adenosine Kinases
    Summary: Adenosine kinase inhibitor,potent
      ≥83 mg/mL
  5. Fluoxetine HCl
    A2436 Fluoxetine HCl
    Target: Serotonin (5-HT) reuptake
    Summary: Serotonin reuptake inhibitor,selective
      insoluble in H2O; ≥17.3 mg/mL
  6. kobe2602
    B3587 kobe2602
    Summary: Ras inhibitor
      insoluble in H2O; ≥17 mg/mL
  7. Fluvoxamine
    B1205 Fluvoxamine
    Target: Serotonin reuptake
    Summary: Selective serotonin reuptake inhibitor
      insoluble in H2O; ≥15.92 mg/mL
  8. Reparixin L-lysine salt
    A3753 Reparixin L-lysine salt
     1 Citation
    Target: CXCR
    Summary: CXCR1/CXCR2 inhibitor
      insoluble in DMSO; ≥16.67 mg/mL
  9. Reparixin
    A3752 Reparixin
     1 Citation
    Target: CXCR
    Summary: Inhibitor of CXCL8 receptor and CXCR1/CXCR2 activation
      insoluble in H2O; ≥14.15 mg/mL
  10. SEA0400
    A3811 SEA0400
     4 Citation
    Target: Na /Ca2 Exchangers (NCXs)
    Summary: Specific inhibitor of Na+/Ca2+ exchange
      insoluble in H2O; ≥18.57 mg/mL

Items 1-10 of 18

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