Thalidomide-piperidin-O-piperidin TFA is an E3 ligase ligand-linker conjugate designed for the synthesis of PROTAC (proteolysis-targeting chimeras). This compound features a CRBN-based ligand linked to a piperidine moiety, facilitating targeted protein degradation. It serves as a valuable tool in chemical biology and drug discovery, particularly for studying protein regulation and therapeutic modulation of disease-related proteins.
Thalidomide-piperidin-O-piperidin TFA is an E3 ligase ligand-linker conjugate designed for the synthesis of PROTAC (proteolysis-targeting chimeras). This compound features a CRBN-based ligand linked to a piperidine moiety, facilitating targeted protein degradation. It serves as a valuable tool in chemical biology and drug discovery, particularly for studying protein regulation and therapeutic modulation of disease-related proteins.
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