Cycloalkenyl hydroxamic acid derivatives and their use as histone deacetylase inhibitors
Abstract:
The present invention provides compounds of formula (I): or a pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein W, X, n, s, t, and Ra are as described herein. The present invention relates generally to selective inhibitors of histone deacetylase and to methods of making and using them.
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