HDAC6-IN-66 is a potent and selective inhibitor of histone deacetylase 6 (HDAC6), exhibiting an IC50 of 1.8 nM. This compound effectively induces acetylation of α-tubulin while preferentially impacting histone H3. HDAC6-IN-66 serves as a valuable tool for cancer research, facilitating studies on the role of HDAC6 in oncogenic processes and potential therapeutic interventions.
HDAC6-IN-66 is a potent and selective inhibitor of histone deacetylase 6 (HDAC6), exhibiting an IC50 of 1.8 nM. This compound effectively induces acetylation of α-tubulin while preferentially impacting histone H3. HDAC6-IN-66 serves as a valuable tool for cancer research, facilitating studies on the role of HDAC6 in oncogenic processes and potential therapeutic interventions.
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