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SIS17 is an inhibitor of histone deacetylase 11 (HDAC11; IC50 = 0.83 µM).1 It is selective for HDAC11 over HDAC1, -4, and -8 (IC50s = >100 µM for all) and sirtuin 1 (SIRT1), -2, -3, and -6 (IC50s = >100 µM for all). SIS17 (50 µM) increases fatty acylation of serine hydroxymethyltransferase 2 (SHMT2) in MCF-7 cells. It decreases the viability of K562 cells and enhances reductions in cell viability induced by oxaliplatin (Item No. 13106) in the same cells.2
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