MI-773

CAT:
804-HY-17493-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
MI-773 - image 1

MI-773

  • Description :

    MI-773 is a potent MDM2-p53 protein‐protein interaction (PPI) inhibitor with high binding affinity against MDM2 (Kd=8.2 nM) . MI-773 has antitumor activity[1][2].
  • UNSPSC :

    12352005
  • Hazard Statement :

    H302, H315, H320, H335
  • Target :

    E1/E2/E3 Enzyme; MDM-2/p53
  • Type :

    Reference compound
  • Related Pathways :

    Apoptosis; Metabolic Enzyme/Protease
  • Applications :

    Cancer-Kinase/protease
  • Field of Research :

    Cancer
  • Assay Protocol :

    https://www.medchemexpress.com/MI-773.html
  • Concentration :

    10mM
  • Purity :

    98.0
  • Solubility :

    DMSO : ≄ 53 mg/mL
  • Smiles :

    O=C([C@H](N[C@@H]1CC(C)(C)C)[C@H](C2=CC=CC(Cl)=C2F)[C@]31C(NC4=C3C=CC(Cl)=C4)=O)N[C@H]5CC[C@H](O)CC5
  • Molecular Formula :

    C29H34Cl2FN3O3
  • Molecular Weight :

    562.50
  • Precautions :

    H302, H315, H320, H335
  • References & Citations :

    [1]Zhang Q, et al. Targeting p53-MDM2-MDMX loop for cancer therapy. Subcell Biochem. 2014;85:281-319.|[2]Tatyana A Grigoreva, et al. Amino acids as chiral derivatizing agents for antiproliferative substituted N-benzyl isoindolinones. Chirality. 2018 Jun;30 (6) :785-797.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    4°C (Powder, stored under nitrogen)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    No Development Reported
  • CAS Number :

    [1303607-07-9]

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