RD-23 is an orally active and selective RET PROTAC degrader, with DC 50 values of 5.6 nM and 11.7 nM against RET WT and RET G810C mutants, respectively. RD-23 inhibits purified RET kinase activity with an IC 50 of 0.371 nM. RD-23 suppresses the activation of downstream Shc signaling and induces apoptosis . RD-23 can be used for the research of RET-related cancers. (Pink: RET ligand ( HY-168868 ); Blue: Cereblon ligand ( HY-43722 ); Black: linker ( HY-W010642 )).
Products | Products > Disease Areas > Cancer | Products > Signaling Pathways > PROTAC | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Signaling Pathways > Apoptosis | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Immunotherapy | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Research Areas > Cancer | Products > Signaling Pathways > PROTACs | Products > Signaling Pathways > RET | Products > Signaling Pathways > Apoptosis
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