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- W2951245998 abstract "A docking protocol using Gold software was developed to predict the binding disposition of histone deacetylase (HDAC) inhibitors, starting from the X-ray structures of HDAC8. The optimized procedure was subsequently utilized to dock into HDAC8 and into a homology model of HDAC1 nearly 40 compounds that had been tested for their inhibitory activity against the two HDAC isozymes. Evaluation of the best binding poses allowed us to identify the ligand properties and the protein residues important for activity and selectivity. HDACs are important anticancer drug targets, and their study is currently being actively pursued. As such, our results could help design new isozyme-selective HDAC inhibitors. Furthermore, this strategy may also be used for the investigation of other HDACs." @default.
- W2951245998 created "2019-06-27" @default.
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- W2951245998 date "2010-03-30" @default.
- W2951245998 modified "2023-09-27" @default.
- W2951245998 title "ChemInform Abstract: Docking of Hydroxamic Acids into HDAC1 and HDAC8: A Rationalization of Activity Trends and Selectivities." @default.
- W2951245998 cites W2064804942 @default.
- W2951245998 doi "https://doi.org/10.1002/chin.201013215" @default.
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