(S)-Thalidomide-azetidine-O-Pip is an E3 ligase ligand-linker conjugate designed for targeted protein degradation via the knockdown of specific proteins. This compound features a CRBN-based ligand that enables the selective recruitment of E3 ligases, facilitating the formation of PROTACs (PROteolysis TArgeting Chimeras). It is valuable in studies focused on therapeutic strategies, cancer research, and functional proteomics.
(S)-Thalidomide-azetidine-O-Pip is an E3 ligase ligand-linker conjugate designed for targeted protein degradation via the knockdown of specific proteins. This compound features a CRBN-based ligand that enables the selective recruitment of E3 ligases, facilitating the formation of PROTACs (PROteolysis TArgeting Chimeras). It is valuable in studies focused on therapeutic strategies, cancer research, and functional proteomics.
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