TMX-3013 is a CDK inhibitor capable of inhibiting the activity of CDK1 , CDK2 , CDK4 , CDK5 , and CDK6 , with IC 50 values of 0.9 nM, <0.5 nM, 24.5 nM, 0.5 nM, and 15.6 nM, respectively. TMX-3013 can be used as a target protein ligand , conjugated with the PROTAC linker and the CRBN ligand Thalidomide ( HY-14658 ) for the synthesis of PROTAC TMX-2138 ( HY-164906 ). TMX-3013 can also act as an effector ligand, binding to target proteins HaloTag or FKBP , and can be used in the synthesis of regulated induced proximity targeting chimeras (RIPTACs).
Products | Products > Disease Areas > Cancer | Products > Signaling Pathways > PROTAC | Products > Signaling Pathways > Cell Cycle/DNA Damage | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Signaling Pathways > Ligands for Target Protein for PROTAC | Products > Signaling Pathways > CDK
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