HJM-561 is a selective and effective orally active EGFR PROTAC degrader. HJM-561 is able to overcome the triple EGFR mutations that are resistant to Osimertinib ( HY-15772 ). HJM-561 exhibits potent degradation of EGFR Del19/T790M/C797S ( DC 50 : 9.2 nM) and L858R/T790M/C797S ( DC 50 : 5.8 nM), and has anti-tumor activity (pink: EGFR ligand ( HY-12857 ); blue: CRBN ligand ( HY-A0003 ); black: linker).
Products | Products > Disease Areas > Cancer | Products > Signaling Pathways > PROTAC | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Signaling Pathways > JAK/STAT Signaling | Products > Research Areas > Cancer > Cancer Drug Resistance | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Signaling Pathways > PROTACs | Products > Signaling Pathways > EGFR
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