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Data from: Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors

Citation

Wang, Fang et al. (2019), Data from: Nɛ-acetyl lysine derivatives with zinc binding groups as novel HDAC inhibitors, Dryad, Dataset, https://doi.org/10.5061/dryad.d1t59pp

Abstract

HDAC inhibitors have been developed very rapidly in clinical trials and even in approvals for treating several cancers. However, there are few reported HDAC inhibitors designed from Nε-acetyl lysine. In current study, we raised a novel design, which is about Nε-acetyl lysine analogues containing amide acetyl groups with the hybridization of ZBG groups as novel HDAC inhibitors.

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