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Anhui Univ. of Chinese Medicine HDAC6 compound 59: sourced facts only. name: "SAR study culminated in the discovery of compound 59, which exhibited remarkable inhibitory activity against both PI3Kδ (IC50 = 2.3 nM) and HDAC6 (IC50 = 13 nM), along with acceptable subtype specificity." [PMID:36182802]; target: "SAR study culminated in the discovery of compound 59, which exhibited remarkable inhibitory activity against both PI3Kδ (IC50 = 2.3 nM) and HDAC6 (IC50 = 13 nM), along with acceptable subtype specificity." [PMID:36182802]; developer: "School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China." [PMID:36182802]
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