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  • Search results for: 'research area cell cycle c myc'

Search results for: 'research area cell cycle c myc'

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  1. PluriSIn #1 (NSC 14613)
    A4351 PluriSIn #1 (NSC 14613)
    Target: Stearoyl-CoA 9-desaturase (SCD-1)
    Summary: SCD1 inhibitor
  2. AT13387
    A4056 AT13387
    Target: HSP90
    Summary: Hsp90 inhibitor
      insoluble in H2O; ≥13.25 mg/mL
  3. U-73122
    B3422 U-73122
     1 Citation
    Target: PC-PLC
    Summary: inhibitor of phospholipase C, phospholipase A2, and 5-LO (5-lipoxygenase)
  4. L-165041
    A3536 L-165041
    Target: PPAR
    Summary: PPARβ/δ agonist,cell permeable,potent and selective
      ≥40.2 mg/mL
  5. Posaconazole
    A1718 Posaconazole
    Target: Cytochrome P450 (CYP450)|sterol demethylase
    Summary: Sterol C14ɑ demethylase inhibitor
      ≥35.04 mg/mL
  6. BMS 309403
    B7794 BMS 309403
     2 Citation
    Target: Fatty-acid-binding proteins (FABPs)
    Summary: FABP4 inhibitor,potent and selective
      insoluble in H2O; ≥18.15 mg/mL
  7. Elesclomol (STA-4783)
    A4386 Elesclomol (STA-4783)
     3 Citation
    Summary: Oxidative stress/apoptosis inducer,potent and novel
      insoluble in H2O; ≥20.15 mg/mL
  8. Glibenclamide
    B1296 Glibenclamide
    Target: Inward Rectifier Potassium (Kir) Channels
    Summary: Insulin production modulator
      ≥49.4 mg/mL
  9. Apremilast (CC-10004)
    A4317 Apremilast (CC-10004)
    Target: Phosphodiesterases (PDEs)
    Summary: PDE4 inhibitor
      ≥23.05 mg/mL
  10. Cilomilast
    A4329 Cilomilast
    Target: Phosphodiesterases (PDEs)
    Summary: Potent PDE4 inhibitor
      insoluble in H2O; ≥12.95 mg/mL

Items 1-10 of 11

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