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Scriptaid is a small molecule histone deacetylase (HDAC) inhibitor that was one of the first compounds discovered via high-throughput screening to act at this target. It is a cell-permeable hydroxamic acid derivative with relatively low toxicity. Scriptaid has been primarily researched for its anti-tumor properties and as a radiosensitizer in cancer models, where it enhances the response of tumor cells to radiation by inhibiting DNA double-strand break repair and suppressing Ku80 expression. While not developed for clinical use itself, it has served as a lead compound for the development of other HDAC inhibitors such as vorinostat. Beyond oncology research, Scriptaid has also been used in studies related to cloning and metabolic regulation[1][2][4][6].
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