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Updated: Oct 25, 2026

Simultaneous Measurement of HDAC1 and HDAC6 Activity in HeLa Cells Using UHPLC-MS
Published on: August 10, 2017
HDACiAP: A Curated Database and Analytical Platform for Histone Deacetylase Inhibitors
Yuhe Xiao1,2, Jiaping Ou1,2, Jiatong Chen1,2
1Key Laboratory of Tropical Medicinal Resource Chemistry of Ministry of Education, Key Laboratory of Tropical Medicinal Plant Chemistry of Hainan Province, School of Chemistry and Chemical Engineering, Hainan Normal University, Haikou, Hainan571158, P. R. China.
Abstract:
Histone deacetylases (HDACs) are pivotal epigenetic regulators that are aberrantly expressed in various cancers, making them prominent targets for anticancer drug development. Herein, we present HDACiAP (https://hdac.kangsgo.cn), a meticulously curated, comprehensive database and analytical platform dedicated to HDAC inhibitors. HDACiAP currently encompasses 32,721 compounds with 123,154 bioactivity records, integrating multidimensional data such as physicochemical properties, biological activities, toxicity predictions, compound selectivity annotations, computationally generated docking poses, and protein-ligand interaction profiles. The platform incorporates built-in molecular docking and integrated machine learning and deep learning-based prediction modules, enabling users to evaluate the potency of novel compounds. Additionally, HDACiAP offers an intuitive visualization interface, multimodal search capabilities, and programmatic access via RESTful APIs. In summary, by providing a curated bioactivity resource together with computational docking annotations and predictive models, HDACiAP offers a practical platform for exploring HDAC inhibitor chemical space, supporting preliminary virtual screening, and facilitating AI-assisted discovery of HDAC-targeted compounds.
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