Desamino lenalidomide-Pip-azetidine hydrochloride is an E3 ligase ligand-linker conjugate that utilizes a cereblon (CRBN)-based ligand in conjunction with a linker moiety. This compound facilitates the synthesis of PROTACs (proteolysis-targeting chimeras), which can selectively target and degrade specific proteins within cellular systems. Its application in drug discovery and development enhances the understanding of protein regulation and degradation pathways.
Desamino lenalidomide-Pip-azetidine hydrochloride is an E3 ligase ligand-linker conjugate that utilizes a cereblon (CRBN)-based ligand in conjunction with a linker moiety. This compound facilitates the synthesis of PROTACs (proteolysis-targeting chimeras), which can selectively target and degrade specific proteins within cellular systems. Its application in drug discovery and development enhances the understanding of protein regulation and degradation pathways.
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