HDAC3-IN-4 is a selective and orally active HDAC3 inhibitor with an IC 50 of 89 nM. HDAC3-IN-4 induces the degradation of PD-L1 by regulating cathepsin B (CTSB) in the lysosomes, with a DC 50 of 5.7 μM. HDAC3-IN-4 shows better selectivity for HDAC3 over HDAC1 , HDAC6 , HDAC7 , and HDAC8 .
Products | Products > Signaling Pathways > Cell Cycle/DNA Damage | Products > Signaling Pathways > Epigenetics | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Signaling Pathways > HDAC
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