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ARV-471 is a proteolysis-targeting chimera (PROTAC) containing a derivative of the estrogen receptor (ER) modulator lasofoxifene conjugated to the immunomodulatory cereblon ligand lenalidomide (Cay-14643). It induces degradation of ER in MCF-7 breast cancer cells with a half-maximal degradation concentration (DC50) value of 0. nM. ARV-471 also induces degradation of ER in cells expressing a variety of clinically relevant ER mutants. It inhibits the growth of T47D triple-negative breast cancer cells and MCF-7 cells expressing wild-type ER (GI50s = 4. and 3. nM, respectively) and T47D cells expressing ERY537S or ERD538G hormone-independent activating mutations (GI50s = 8 and 5. nM, respectively). ARV-471 (3, 10, and 30 mg/kg per day) reduces tumor growth in an MCF-7 orthotopic mouse xenograft model. It induces tumor regression in a patient-derived xenograft (PDX) ERY537S-expressing mouse model of breast cancer when administered at doses of 10 and 30 mg/kg.. Solulibility: H2O: Slightly soluble: 0.1-1 mg/ml: .
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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