Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More
Learn More
Medchemexpress LLC Protac ER degrader-4 | 2361114-15-8 | 98.8% | C53H67F3N6O8S | 10MG
Supplier: Medchemexpress LLC HY13530910MG
PROTAC ER Degrader-4 is a von Hippel-Lindau (VHL)-based proteolysis-targeting chimera that binds and induces degradation of the estrogen receptor (ER) in biochemical and cellular assays. It exhibits potent ER binding (IC50 0.8 nM) and induces ER degradation in MCF-7 cells (IC50 0.3 nM); supplied as a high-purity research compound for mechanistic studies of ER biology.
- VHL-based PROTAC mechanism of action.
- Potent ER binding (IC50 0.8 nM) and degradation in MCF-7 cells (IC50 0.3 nM).
- High purity suitable for biochemical and cell-based studies.
- Available in small research quantities.
- Recommended storage at -20°C under inert gas; long-term stability in solvent at -80°C.
Product Title
By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.
Spot an opportunity for improvement?