SHP2-D26

CAT:
804-HY-145162-01
Size:
1 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
SHP2-D26 - image 1

SHP2-D26

  • Description:

    SHP2-D26 is a first, potent and effective SHP2 PROTAC degrader. SHP2-D26 induces SHP2 degradation requires binding to VHL-1 and SHP2 proteins. SHP2-D26 is also neddylation- and proteasome-dependent. SHP2-D26 can be used for the study of esophageal cancer and acute myeloid leukemia (Pink: SHP2 ligand (HY-176797) ; Blue: VHL ligand (HY-150803) ; Black: linker) [1].
  • UNSPSC:

    12352005
  • Target:

    Phosphatase; PROTACs; SHP2
  • Type:

    Reference compound
  • Related Pathways:

    Metabolic Enzyme/Protease; PROTAC; Protein Tyrosine Kinase/RTK
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/shp2-d26.html
  • Purity:

    95.83
  • Solubility:

    DMSO : 83.33 mg/mL (ultrasonic)
  • Smiles:

    ClC(C(SC1=NC=C(N2CCC(N)(CC2)C)N=C1N)=CC=C3)=C3NC(CCC(N(CC4)CCN4CCCCCCCCC(N[C@@H](C(C)(C)C)C(N5[C@@H](C[C@H](C5)O)C(N[C@H](C6=CC=C(C7=C(C)N=CS7)C=C6)C)=O)=O)=O)=O)=O
  • Molecular Formula:

    C56H79ClN12O6S2
  • Molecular Weight:

    1115.89
  • References & Citations:

    [1]Wang M, et al. Discovery of SHP2-D26 as a First, Potent, and Effective PROTAC Degrader of SHP2 Protein [published correction appears in J Med Chem. 2021 Jan 14;64 (1) :906-908]. J Med Chem. 2020;63 (14) :7510-7528.|[2]Wang M, et al. Correction to "Discovery of SHP2-D26 as a First, Potent, and Effective PROTAC Degrader of SHP2 Protein". J Med Chem. 2021 Jan 14;64 (1) :906-908.
  • 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:

    [2458219-65-1]