DDC-01-163

DDC-01-163
  • CAS No.:2140806-84-2
  • Grade:99.05%
  • Formula:C49H51N9O9S
  • M.W.:942.05

Overview

DDC-01-163 is an allosteric PROTAC degrader targeting EGFR . DDC-01-163 is dependent on the ubiquitin–proteasome system. DDC-01-163 can selectively inhibit the proliferation of L858R/T790M (L/T) mutant Ba/F3 cells. DDC-01-163 is effective against Osimertinib ( HY-15772 )-resistant cells with L/T/C797S and L/T/L718Q EGFR mutations. DDC-01-163 exhibits enhanced anti-proliferative activity against L858R/T790M EGFR-Ba/F3 cells when combined with the ATP-site EGFR inhibitor Osimertinib . DDC-01-163 can be used for the study of non-small cell lung cancer . (Pink: EGFR ligand ( HY-151048 ); Blue: Cereblon ligand ( HY-14658 ); Black: linker ( HY-W008005 )).

Application

Products | Products > Disease Areas > Respiratory Cancer | Products > Disease Areas > Non-Small Cell Lung Cancer | Products > Disease Areas > Cancer | Products > Disease Areas > Respiratory Disease | Products > Disease Areas > Lung Cancer | Products > Signaling Pathways > PROTAC | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Signaling Pathways > JAK/STAT Signaling | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Immunotherapy | Products > Research Areas > Cancer > Cancer Drug Resistance | Products > Signaling Pathways > PROTACs | Products > Signaling Pathways > EGFR

Product Information

  • Catalog No.: HY-139997
  • CAS No.: 2140806-84-2
  • Molecular Formula: C49H51N9O9S
  • Molecular Weight: 942.05
  • Purity: 99.05%
  • Storage: Powder -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
  • Availability: In-stock

Source

Original product source


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