Thalidomide-O-PEG4-acid is a PROTAC linker designed for targeted protein degradation applications. It features a reactive site for amine-containing moieties, enabling efficient conjugation in the presence of coupling agents such as EDC or HATU. This compound is crucial for the development of bifunctional molecules that facilitate the selective degradation of target proteins, supporting research in cancer, neurodegenerative diseases, and cellular regulation.
Thalidomide-O-PEG4-acid is a PROTAC linker designed for targeted protein degradation applications. It features a reactive site for amine-containing moieties, enabling efficient conjugation in the presence of coupling agents such as EDC or HATU. This compound is crucial for the development of bifunctional molecules that facilitate the selective degradation of target proteins, supporting research in cancer, neurodegenerative diseases, and cellular regulation.
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