N-Hydroxyphthalimide

CAT:
804-HY-Y0396-01
Size:
50 g
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
N-Hydroxyphthalimide - image 1

N-Hydroxyphthalimide

  • Description:

    N-Hydroxyphthalimide is a blocking agent and catalyst. N-Hydroxyphthalimide promotes oxidation reactions by generating PINO free radicals and activating hydrogen atom transfer processes. N-Hydroxyphthalimide reduces the expression of anti-apoptotic proteins Survivin and Bcl-xL and activates caspase 9 and caspase 3. N-Hydroxyphthalimide induces Apoptosis. N-Hydroxyphthalimide inhibits the phosphorylation of mTOR (Ser2448, Ser2481) and Akt (Ser473) . N-Hydroxyphthalimide has anticancer effects against breast and colon cancer[1][2][3].
  • UNSPSC:

    12352200
  • Hazard Statement:

    H302, H315, H319, H335
  • Target:

    Akt; Apoptosis; Bcl-2 Family; Biochemical Assay Reagents; Caspase; mTOR; Survivin
  • Type:

    Biochemical Assay Reagents
  • Related Pathways:

    Apoptosis; Others; PI3K/Akt/mTOR
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/n-hydroxyphthalimide.html
  • Purity:

    99.89
  • Solubility:

    DMSO : 100 mg/mL (ultrasonic)
  • Smiles:

    O=C1C2=C(C(N1O)=O)C=CC=C2
  • Molecular Formula:

    C8H5NO3
  • Molecular Weight:

    163.13
  • Precautions:

    H302, H315, H319, H335
  • References & Citations:

    [1]Wei W J, et al. Study on N‐hydroxyphthalimide as blocking agent for isocyanates. Journal of applied polymer science, 2002, 84 (7) : 1346-1352. |[2]Melone L, et al. N-Hydroxyphthalimide catalysts as bioactive pro-oxidants. RSC Advances, 2016, 6 (26) : 21749-21755. |[3]Wang M, et al. N-Hydroxyphthalimide exhibits antitumor activity by suppressing mTOR signaling pathway in BT-20 and LoVo cells. J Exp Clin Cancer Res. 2016 Mar 3;35:41.
  • Shipping Conditions:

    Room Temperature
  • Storage Conditions:

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

    Biochemical Assay Reagents
  • Clinical Information:

    No Development Reported
  • Isoform:

    Bcl-xL; Caspase 3; Caspase 9
  • CAS Number:

    524-38-9