ES-072

Overview

ES-072 is an orally effective selective EGFR mutant ( EGFR-T790M ) inhibitor. ES-072 activates GSK3α by inhibiting EGFR-T790M activity, which promotes phosphorylation of PD-L1 at Ser279 and Ser283. The phosphorylated PD-L1 recruits the E3 ubiquitin ligase ARIH1 , leading to ubiquitination and proteasomal degradation of PD-L1 . This mechanism not only reduces cancer cell growth but also enhances anti-tumor immune response by lowering PD-L1 levels. ES-072 can be used to inhibit proliferation in non-small cell lung cancer (NSCLC) cells.

Application

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Product Information

• Catalog No.: HY-164476
• CAS No.: 2089721-94-6
• Molecular Formula: C25H27F3N8O2
• Molecular Weight: 528.53
• Purity: 98.05%
• Storage: Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
• Solubility: ≥ 2.5 mg/mL (4.73 mM); Clear solution
• Availability: In-stock

Source

Original product source