HDAC-IN-52 is a pyridine-based inhibitor targeting histone deacetylases (HDACs) with IC50 values of 0.189 μM for HDAC1, 0.227 μM for HDAC2, 0.440 μM for HDAC3, and 0.446 μM for HDAC10. This compound exhibits potent HDAC inhibition, making it a valuable tool for investigating epigenetic regulation in cancer research. Its application extends to the study of cell differentiation, apoptosis, and potential therapeutic strategies in oncology.
HDAC-IN-52 is a pyridine-based inhibitor targeting histone deacetylases (HDACs) with IC50 values of 0.189 μM for HDAC1, 0.227 μM for HDAC2, 0.440 μM for HDAC3, and 0.446 μM for HDAC10. This compound exhibits potent HDAC inhibition, making it a valuable tool for investigating epigenetic regulation in cancer research. Its application extends to the study of cell differentiation, apoptosis, and potential therapeutic strategies in oncology.
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