PROTAC ERα Degrader-2

CAT:
804-HY-111846-01
Size:
5 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
PROTAC ERα Degrader-2 - image 1

PROTAC ERα Degrader-2

  • CAS Number:

    1351169-29-3
  • UNSPSC Description:

    PROTAC ERα Degrader-2 comprises a IAP ligand binding group, a linker and an estrogen receptor α (ERα) binding group. PROTAC ERα Degrader-2 is an ERα degrader. Maximal ERα degradation at 30 μM concentration in human mammary tumor MCF7 cells. Degradation inducers based on cIAP1 are called specific and non-genetic IAP-dependent protein erasers (SNIPERs)[1].
  • Target Antigen:

    Estrogen Receptor/ERR; PROTACs; SNIPERs
  • Type:

    Reference compound
  • Related Pathways:

    PROTAC;Vitamin D Related/Nuclear Receptor
  • Applications:

    Cancer-programmed cell death
  • Field of Research:

    Cancer
  • Assay Protocol:

    https://www.medchemexpress.com/protac-er-alpha-degrader-2.html
  • Purity:

    98.92
  • Solubility:

    DMSO : 200 mg/mL (ultrasonic)
  • Smiles:

    C[C@@]12[C@](CC/C2=N\OCC(NCCOCCOCCNC([C@H](CC(C)C)NC([C@@H](O)[C@H](N)CC3=CC=CC=C3)=O)=O)=O)([H])[C@@]4([H])[C@](C5=CC=C(O)C=C5CC4)([H])CC1
  • Molecular Weight:

    763.96
  • References & Citations:

    [1]Scheepstra M, et al. Bivalent Ligands for Protein Degradation in Drug Discovery. Comput Struct Biotechnol J. 2019 Jan 25;17:160-176.
  • Shipping Conditions:

    Blue Ice
  • Storage Conditions:

    -20°C (Powder, stored under nitrogen)
  • Clinical Information:

    No Development Reported