Thalidomide-O-amido-C6-NH2 serves as an E3 ligase ligand-linker conjugate, featuring a thalidomide-based cereblon ligand with an integrated linker. This compound is utilized in the synthesis of PROTACs (proteolysis-targeting chimeras), facilitating targeted protein degradation pathways. Its unique structure allows for selective degradation of specific proteins, making it valuable in cancer research and other therapeutic applications.
Thalidomide-O-amido-C6-NH2 serves as an E3 ligase ligand-linker conjugate, featuring a thalidomide-based cereblon ligand with an integrated linker. This compound is utilized in the synthesis of PROTACs (proteolysis-targeting chimeras), facilitating targeted protein degradation pathways. Its unique structure allows for selective degradation of specific proteins, making it valuable in cancer research and other therapeutic applications.
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