Thalidomide-5-F-6-azetidin-MeOH is an E3 ligase ligand-linker conjugate, specifically designed for the synthesis of PROTAC FLT3/CHK1 Degrader-1. This compound effectively targets and degrades FLT3 and CHK1, demonstrating significant anti-tumor activity. It serves as a valuable tool in drug development research, facilitating insights into targeted protein degradation mechanisms in cancer therapy.
Thalidomide-5-F-6-azetidin-MeOH is an E3 ligase ligand-linker conjugate, specifically designed for the synthesis of PROTAC FLT3/CHK1 Degrader-1. This compound effectively targets and degrades FLT3 and CHK1, demonstrating significant anti-tumor activity. It serves as a valuable tool in drug development research, facilitating insights into targeted protein degradation mechanisms in cancer therapy.
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