Thalidomide-NH-C2-2-azaspiro[3.3]heptane is a conjugate designed for targeting E3 ubiquitin ligases and serves as a linker component in the development of bifunctional degradation technologies. This compound plays a crucial role in the synthesis of KT-413, facilitating selective protein degradation for research applications in cancer and other diseases. Its unique structure enhances ligand-receptor interactions, offering valuable insights into E3 ligase biology and therapeutic targeting.
Thalidomide-NH-C2-2-azaspiro[3.3]heptane is a conjugate designed for targeting E3 ubiquitin ligases and serves as a linker component in the development of bifunctional degradation technologies. This compound plays a crucial role in the synthesis of KT-413, facilitating selective protein degradation for research applications in cancer and other diseases. Its unique structure enhances ligand-receptor interactions, offering valuable insights into E3 ligase biology and therapeutic targeting.
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