S49076

CAT:
804-HY-12965-01
Size:
2 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
S49076 - image 1

S49076

  • Description :

    S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3 with IC50 values below 20 nM.
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302
  • Target :

    C-Met/HGFR; FGFR
  • Type :

    Reference compound
  • Related Pathways :

    Protein Tyrosine Kinase/RTK
  • Applications :

    Cancer-Kinase/protease
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/S49076.html
  • Concentration :

    10mM
  • Purity :

    99.44
  • Solubility :

    DMSO : ≥ 31 mg/mL
  • Smiles :

    O=C(N1CC2=CC3=C(NC(/C3=C\C4=CC(CN5CCOCC5)=CN4)=O)C=C2)SCC1=O
  • Molecular Formula :

    C22H22N4O4S
  • Molecular Weight :

    438.50
  • Precautions :

    H302
  • References & Citations :

    [1]Burbridge MF, et al. S49076 is a novel kinase inhibitor of MET, AXL, and FGFR with strong preclinical activity alone and in association with bevacizumab. Mol Cancer Ther. 2013 Sep;12 (9) :1749-62.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [1265965-22-7]

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