2-(2,6-Dioxopiperidin-3-yl)phthalimidine-azetidine is an E3 ligase ligand-linker conjugate that incorporates a CRBN-based ligand. This compound plays a pivotal role in the synthesis of Proteolysis Targeting Chimeras (PROTACs), facilitating the targeted degradation of specific proteins. Its structure enables efficient binding to E3 ligases, making it a valuable tool for research in protein degradation strategies and therapeutic development.
2-(2,6-Dioxopiperidin-3-yl)phthalimidine-azetidine is an E3 ligase ligand-linker conjugate that incorporates a CRBN-based ligand. This compound plays a pivotal role in the synthesis of Proteolysis Targeting Chimeras (PROTACs), facilitating the targeted degradation of specific proteins. Its structure enables efficient binding to E3 ligases, making it a valuable tool for research in protein degradation strategies and therapeutic development.
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